Canonical Allele Identifier: CA16602783
Community Standard Title: NM_004304.5(ALK):c.3467G>A (p.Cys1156Tyr)
Gene: ALK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29222392C>T , CM000664.2:g.29222392C>T GRCh38
NC_000002.11:g.29445258C>T , CM000664.1:g.29445258C>T GRCh37
NC_000002.10:g.29298762C>T NCBI36
NG_009445.1:g.704175G>A , LRG_488:g.704175G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004304.5:c.3467G>A MANE Select NP_004295.2:p.Cys1156Tyr
ENST00000389048.8:c.3467G>A MANE Select ENSP00000373700.3:p.Cys1156Tyr
NM_001353765.1:c.263G>A NP_001340694.1:p.Cys88Tyr
NM_001353765.2:c.263G>A NP_001340694.1:p.Cys88Tyr
NM_004304.4:c.3467G>A NP_004295.2:p.Cys1156Tyr
ENST00000389048.7:c.3467G>A ENSP00000373700.3:p.Cys1156Tyr
ENST00000431873.5:c.347G>A ENSP00000414027.2:p.Cys116Tyr
ENST00000431873.6:c.694G>A
ENST00000453137.1:c.161G>A ENSP00000387488.1:p.Cys54Tyr
ENST00000618119.4:c.2336G>A ENSP00000482733.1:p.Cys779Tyr
ENST00000638605.1:n.344G>A
ENST00000642122.1:c.263G>A ENSP00000493203.1:p.Cys88Tyr
XM_024452778.1:c.620G>A XP_024308546.1:p.Cys207Tyr
XM_024452779.1:c.263G>A XP_024308547.1:p.Cys88Tyr
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