Canonical Allele Identifier: CA421821577

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873159C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904021C>G , CM000663.2:g.173904021C>G	GRCh38
NC_000001.10:g.173873159C>G , CM000663.1:g.173873159C>G	GRCh37
NC_000001.9:g.172139782C>G	NCBI36
NG_012462.1:g.18358G>C , LRG_577:g.18358G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1263G>C MANE Select	ENSP00000356671.3:p.Val421=
ENST00000367698.3:c.1263G>C	ENSP00000356671.3:p.Val421=
ENST00000617423.4:c.648G>C	ENSP00000478688.1:p.Val216=
NM_000488.3:c.1263G>C , LRG_577t1:c.1263G>C	NP_000479.1:p.Val421=
XM_005245198.2:c.1119G>C	XP_005245255.1:p.Val373=
NM_001365052.1:c.1119G>C	NP_001351981.1:p.Val373=
NM_000488.4:c.1263G>C MANE Select	NP_000479.1:p.Val421=
NM_001365052.2:c.1119G>C	NP_001351981.1:p.Val373=
NM_001386302.1:c.1386G>C	NP_001373231.1:p.Val462=
NM_001386303.1:c.1344G>C	NP_001373232.1:p.Val448=
NM_001386304.1:c.1242G>C	NP_001373233.1:p.Val414=
NM_001386305.1:c.1206G>C	NP_001373234.1:p.Val402=
NM_001386306.1:c.1047G>C	NP_001373235.1:p.Val349=