Canonical Allele Identifier: CA421942971

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878868G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909730G>T , CM000663.2:g.173909730G>T	GRCh38
NC_000001.10:g.173878868G>T , CM000663.1:g.173878868G>T	GRCh37
NC_000001.9:g.172145491G>T	NCBI36
NG_012462.1:g.12649C>A , LRG_577:g.12649C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.975C>A MANE Select	ENSP00000356671.3:p.Ala325=
ENST00000367698.3:c.975C>A	ENSP00000356671.3:p.Ala325=
ENST00000487183.1:n.626C>A
ENST00000617423.4:c.559+2134C>A	ENSP00000478688.1:n.559+2134C>A
NM_000488.3:c.975C>A , LRG_577t1:c.975C>A	NP_000479.1:p.Ala325=
XM_005245198.2:c.831C>A	XP_005245255.1:p.Ala277=
NM_001365052.1:c.831C>A	NP_001351981.1:p.Ala277=
NM_000488.4:c.975C>A MANE Select	NP_000479.1:p.Ala325=
NM_001365052.2:c.831C>A	NP_001351981.1:p.Ala277=
NM_001386302.1:c.1098C>A	NP_001373231.1:p.Ala366=
NM_001386303.1:c.1056C>A	NP_001373232.1:p.Ala352=
NM_001386304.1:c.954C>A	NP_001373233.1:p.Ala318=
NM_001386305.1:c.918C>A	NP_001373234.1:p.Ala306=
NM_001386306.1:c.759C>A	NP_001373235.1:p.Ala253=