Canonical Allele Identifier: CA343774827
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879080C>A (hg19) chr1:g.173909942C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909942C>A , CM000663.2:g.173909942C>A GRCh38
NC_000001.10:g.173879080C>A , CM000663.1:g.173879080C>A GRCh37
NC_000001.9:g.172145703C>A NCBI36
NG_012462.1:g.12437G>T , LRG_577:g.12437G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.763G>T MANE Select ENSP00000356671.3:p.Gly255Cys
ENST00000367698.3:c.763G>T ENSP00000356671.3:p.Gly255Cys
ENST00000487183.1:n.414G>T
ENST00000617423.4:c.559+1922G>T ENSP00000478688.1:n.559+1922G>T
NM_000488.3:c.763G>T , LRG_577t1:c.763G>T NP_000479.1:p.Gly255Cys
XM_005245198.2:c.619G>T XP_005245255.1:p.Gly207Cys
NM_001365052.1:c.619G>T NP_001351981.1:p.Gly207Cys
NM_000488.4:c.763G>T MANE Select NP_000479.1:p.Gly255Cys
NM_001365052.2:c.619G>T NP_001351981.1:p.Gly207Cys
NM_001386302.1:c.886G>T NP_001373231.1:p.Gly296Cys
NM_001386303.1:c.844G>T NP_001373232.1:p.Gly282Cys
NM_001386304.1:c.742G>T NP_001373233.1:p.Gly248Cys
NM_001386305.1:c.763-57G>T NP_001373234.1:n.763-57G>T
NM_001386306.1:c.547G>T NP_001373235.1:p.Gly183Cys
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