Canonical Allele Identifier: CA421821573

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873156A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904018A>G , CM000663.2:g.173904018A>G	GRCh38
NC_000001.10:g.173873156A>G , CM000663.1:g.173873156A>G	GRCh37
NC_000001.9:g.172139779A>G	NCBI36
NG_012462.1:g.18361T>C , LRG_577:g.18361T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1266T>C MANE Select	ENSP00000356671.3:p.Ile422=
ENST00000367698.3:c.1266T>C	ENSP00000356671.3:p.Ile422=
ENST00000617423.4:c.651T>C	ENSP00000478688.1:p.Ile217=
NM_000488.3:c.1266T>C , LRG_577t1:c.1266T>C	NP_000479.1:p.Ile422=
XM_005245198.2:c.1122T>C	XP_005245255.1:p.Ile374=
NM_001365052.1:c.1122T>C	NP_001351981.1:p.Ile374=
NM_000488.4:c.1266T>C MANE Select	NP_000479.1:p.Ile422=
NM_001365052.2:c.1122T>C	NP_001351981.1:p.Ile374=
NM_001386302.1:c.1389T>C	NP_001373231.1:p.Ile463=
NM_001386303.1:c.1347T>C	NP_001373232.1:p.Ile449=
NM_001386304.1:c.1245T>C	NP_001373233.1:p.Ile415=
NM_001386305.1:c.1209T>C	NP_001373234.1:p.Ile403=
NM_001386306.1:c.1050T>C	NP_001373235.1:p.Ile350=