Canonical Allele Identifier: CA343771994

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873031T>C (hg19) ; chr1:g.173903893T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903893T>C , CM000663.2:g.173903893T>C	GRCh38
NC_000001.10:g.173873031T>C , CM000663.1:g.173873031T>C	GRCh37
NC_000001.9:g.172139654T>C	NCBI36
NG_012462.1:g.18486A>G , LRG_577:g.18486A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1391A>G MANE Select	ENSP00000356671.3:p.Lys464Arg
ENST00000367698.3:c.1391A>G	ENSP00000356671.3:p.Lys464Arg
ENST00000617423.4:c.776A>G	ENSP00000478688.1:p.Lys259Arg
NM_000488.3:c.1391A>G , LRG_577t1:c.1391A>G	NP_000479.1:p.Lys464Arg
XM_005245198.2:c.1247A>G	XP_005245255.1:p.Lys416Arg
NM_001365052.1:c.1247A>G	NP_001351981.1:p.Lys416Arg
NM_000488.4:c.1391A>G MANE Select	NP_000479.1:p.Lys464Arg
NM_001365052.2:c.1247A>G	NP_001351981.1:p.Lys416Arg
NM_001386302.1:c.1514A>G	NP_001373231.1:p.Lys505Arg
NM_001386303.1:c.1472A>G	NP_001373232.1:p.Lys491Arg
NM_001386304.1:c.1370A>G	NP_001373233.1:p.Lys457Arg
NM_001386305.1:c.1334A>G	NP_001373234.1:p.Lys445Arg
NM_001386306.1:c.1175A>G	NP_001373235.1:p.Lys392Arg