Canonical Allele Identifier: CA343774725
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173879037T>A (hg19) chr1:g.173909899T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909899T>A , CM000663.2:g.173909899T>A GRCh38
NC_000001.10:g.173879037T>A , CM000663.1:g.173879037T>A GRCh37
NC_000001.9:g.172145660T>A NCBI36
NG_012462.1:g.12480A>T , LRG_577:g.12480A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.806A>T MANE Select ENSP00000356671.3:p.Glu269Val
ENST00000367698.3:c.806A>T ENSP00000356671.3:p.Glu269Val
ENST00000487183.1:n.457A>T
ENST00000617423.4:c.559+1965A>T ENSP00000478688.1:n.559+1965A>T
NM_000488.3:c.806A>T , LRG_577t1:c.806A>T NP_000479.1:p.Glu269Val
XM_005245198.2:c.662A>T XP_005245255.1:p.Glu221Val
NM_001365052.1:c.662A>T NP_001351981.1:p.Glu221Val
NM_000488.4:c.806A>T MANE Select NP_000479.1:p.Glu269Val
NM_001365052.2:c.662A>T NP_001351981.1:p.Glu221Val
NM_001386302.1:c.929A>T NP_001373231.1:p.Glu310Val
NM_001386303.1:c.887A>T NP_001373232.1:p.Glu296Val
NM_001386304.1:c.785A>T NP_001373233.1:p.Glu262Val
NM_001386305.1:c.763-14A>T NP_001373234.1:n.763-14A>T
NM_001386306.1:c.590A>T NP_001373235.1:p.Glu197Val
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