Canonical Allele Identifier: CA343773540

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878728A>T (hg19) ; chr1:g.173909590A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909590A>T , CM000663.2:g.173909590A>T	GRCh38
NC_000001.10:g.173878728A>T , CM000663.1:g.173878728A>T	GRCh37
NC_000001.9:g.172145351A>T	NCBI36
NG_012462.1:g.12789T>A , LRG_577:g.12789T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1115T>A MANE Select	ENSP00000356671.3:p.Leu372His
ENST00000367698.3:c.1115T>A	ENSP00000356671.3:p.Leu372His
ENST00000617423.4:c.560-2097T>A	ENSP00000478688.1:n.560-2097T>A
NM_000488.3:c.1115T>A , LRG_577t1:c.1115T>A	NP_000479.1:p.Leu372His
XM_005245198.2:c.971T>A	XP_005245255.1:p.Leu324His
NM_001365052.1:c.971T>A	NP_001351981.1:p.Leu324His
NM_000488.4:c.1115T>A MANE Select	NP_000479.1:p.Leu372His
NM_001365052.2:c.971T>A	NP_001351981.1:p.Leu324His
NM_001386302.1:c.1238T>A	NP_001373231.1:p.Leu413His
NM_001386303.1:c.1196T>A	NP_001373232.1:p.Leu399His
NM_001386304.1:c.1094T>A	NP_001373233.1:p.Leu365His
NM_001386305.1:c.1058T>A	NP_001373234.1:p.Leu353His
NM_001386306.1:c.899T>A	NP_001373235.1:p.Leu300His