Canonical Allele Identifier: CA1593738861
Gene: SGCD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156508700C= , CM000667.2:g.156508700C= GRCh38
NC_000005.9:g.155935710C= , CM000667.1:g.155935710C= GRCh37
NC_000005.8:g.155868288C= NCBI36
NG_008693.2:g.643357C= , LRG_205:g.643357C=

Transcript Alleles

HGVS Amino-acid change
ENST00000337851.9:c.292C= MANE Select ENSP00000338343.4:p.Pro98=
ENST00000337851.8:c.292C= ENSP00000338343.4:p.Pro98=
ENST00000435422.7:c.289C= ENSP00000403003.2:p.Pro97=
ENST00000517913.5:c.292C= ENSP00000429378.1:p.Pro98=
ENST00000524347.2:c.*156C= ENSP00000430794.1:n.*156C=
NM_000337.5:c.292C= , LRG_205t1:c.292C= NP_000328.2:p.Pro98=
NM_001128209.1:c.289C= NP_001121681.1:p.Pro97=
NM_172244.2:c.292C= NP_758447.1:p.Pro98=
XM_005265966.3:c.292C= XP_005266023.1:p.Pro98=
XM_005265967.1:c.292C= XP_005266024.1:p.Pro98=
XM_006714911.2:c.292C= XP_006714974.1:p.Pro98=
XM_011534621.1:c.289C= XP_011532923.1:p.Pro97=
XM_005265966.5:c.292C= XP_005266023.1:p.Pro98=
XM_005265967.2:c.292C= XP_005266024.1:p.Pro98=
XM_011534621.2:c.289C= XP_011532923.1:p.Pro97=
XM_017009723.2:c.292C= XP_016865212.1:p.Pro98=
XM_017009724.1:c.292C= XP_016865213.1:p.Pro98=
NM_001128209.2:c.289C= NP_001121681.1:p.Pro97=
NM_172244.3:c.292C= NP_758447.1:p.Pro98=
NM_000337.6:c.292C= MANE Select NP_000328.2:p.Pro98=
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