Canonical Allele Identifier: CA343774024

Gene: SERPINC1

Linked Data

• dbSNP Id: rs2102782763
• gnomAD v4: 1-173909731-G-A
• MyVariant Identifiers: chr1:g.173878869G>A (hg19) ; chr1:g.173909731G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909731G>A , CM000663.2:g.173909731G>A	GRCh38
NC_000001.10:g.173878869G>A , CM000663.1:g.173878869G>A	GRCh37
NC_000001.9:g.172145492G>A	NCBI36
NG_012462.1:g.12648C>T , LRG_577:g.12648C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.974C>T MANE Select	ENSP00000356671.3:p.Ala325Val
ENST00000367698.3:c.974C>T	ENSP00000356671.3:p.Ala325Val
ENST00000487183.1:n.625C>T
ENST00000617423.4:c.559+2133C>T	ENSP00000478688.1:n.559+2133C>T
NM_000488.3:c.974C>T , LRG_577t1:c.974C>T	NP_000479.1:p.Ala325Val
XM_005245198.2:c.830C>T	XP_005245255.1:p.Ala277Val
NM_001365052.1:c.830C>T	NP_001351981.1:p.Ala277Val
NM_000488.4:c.974C>T MANE Select	NP_000479.1:p.Ala325Val
NM_001365052.2:c.830C>T	NP_001351981.1:p.Ala277Val
NM_001386302.1:c.1097C>T	NP_001373231.1:p.Ala366Val
NM_001386303.1:c.1055C>T	NP_001373232.1:p.Ala352Val
NM_001386304.1:c.953C>T	NP_001373233.1:p.Ala318Val
NM_001386305.1:c.917C>T	NP_001373234.1:p.Ala306Val
NM_001386306.1:c.758C>T	NP_001373235.1:p.Ala253Val