Canonical Allele Identifier: CA343774410

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878963G>T (hg19) ; chr1:g.173909825G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909825G>T , CM000663.2:g.173909825G>T	GRCh38
NC_000001.10:g.173878963G>T , CM000663.1:g.173878963G>T	GRCh37
NC_000001.9:g.172145586G>T	NCBI36
NG_012462.1:g.12554C>A , LRG_577:g.12554C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.880C>A MANE Select	ENSP00000356671.3:p.Arg294Ser
ENST00000367698.3:c.880C>A	ENSP00000356671.3:p.Arg294Ser
ENST00000487183.1:n.531C>A
ENST00000617423.4:c.559+2039C>A	ENSP00000478688.1:n.559+2039C>A
NM_000488.3:c.880C>A , LRG_577t1:c.880C>A	NP_000479.1:p.Arg294Ser
XM_005245198.2:c.736C>A	XP_005245255.1:p.Arg246Ser
NM_001365052.1:c.736C>A	NP_001351981.1:p.Arg246Ser
NM_000488.4:c.880C>A MANE Select	NP_000479.1:p.Arg294Ser
NM_001365052.2:c.736C>A	NP_001351981.1:p.Arg246Ser
NM_001386302.1:c.1003C>A	NP_001373231.1:p.Arg335Ser
NM_001386303.1:c.961C>A	NP_001373232.1:p.Arg321Ser
NM_001386304.1:c.859C>A	NP_001373233.1:p.Arg287Ser
NM_001386305.1:c.823C>A	NP_001373234.1:p.Arg275Ser
NM_001386306.1:c.664C>A	NP_001373235.1:p.Arg222Ser