Canonical Allele Identifier: CA384152104
Gene: KRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25227333T>C , CM000674.2:g.25227333T>C GRCh38
NC_000012.11:g.25380267T>C , CM000674.1:g.25380267T>C GRCh37
NC_000012.10:g.25271534T>C NCBI36
NG_007524.1:g.28588A>G
NG_007524.2:g.28671A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.112-17422A>G ENSP00000452512.1:n.112-17422A>G
ENST00000685328.1:c.191A>G ENSP00000508921.1:p.Tyr64Cys
ENST00000686877.1:c.*162A>G ENSP00000510431.1:n.*162A>G
ENST00000687356.1:c.112-1560A>G ENSP00000510511.1:n.112-1560A>G
ENST00000688228.1:n.665A>G
ENST00000688940.1:c.191A>G ENSP00000509238.1:p.Tyr64Cys
ENST00000690804.1:c.*152A>G ENSP00000508568.1:n.*152A>G
ENST00000692768.1:c.-8A>G ENSP00000510254.1:n.-8A>G
ENST00000693229.1:c.116A>G ENSP00000509223.1:p.Tyr39Cys
ENST00000256078.10:c.191A>G MANE Plus Clinical ENSP00000256078.5:p.Tyr64Cys
ENST00000311936.8:c.191A>G MANE Select ENSP00000308495.3:p.Tyr64Cys
ENST00000256078.8:c.191A>G ENSP00000256078.4:p.Tyr64Cys
ENST00000311936.7:c.191A>G ENSP00000308495.3:p.Tyr64Cys
ENST00000557334.5:c.112-17422A>G ENSP00000452512.1:n.112-17422A>G
NM_004985.4:c.191A>G NP_004976.2:p.Tyr64Cys
NM_033360.3:c.191A>G NP_203524.1:p.Tyr64Cys
XM_006719069.2:c.191A>G XP_006719132.1:p.Tyr64Cys
XM_011520653.1:c.191A>G XP_011518955.1:p.Tyr64Cys
XM_006719069.4:c.191A>G XP_006719132.1:p.Tyr64Cys
XM_011520653.3:c.191A>G XP_011518955.1:p.Tyr64Cys
NM_001369786.1:c.191A>G NP_001356715.1:p.Tyr64Cys
NM_001369787.1:c.191A>G NP_001356716.1:p.Tyr64Cys
NM_004985.5:c.191A>G MANE Select NP_004976.2:p.Tyr64Cys
NM_033360.4:c.191A>G MANE Plus Clinical NP_203524.1:p.Tyr64Cys
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