Canonical Allele Identifier: CA421942859

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878775G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909637G>T , CM000663.2:g.173909637G>T	GRCh38
NC_000001.10:g.173878775G>T , CM000663.1:g.173878775G>T	GRCh37
NC_000001.9:g.172145398G>T	NCBI36
NG_012462.1:g.12742C>A , LRG_577:g.12742C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1068C>A MANE Select	ENSP00000356671.3:p.Arg356=
ENST00000367698.3:c.1068C>A	ENSP00000356671.3:p.Arg356=
ENST00000617423.4:c.560-2144C>A	ENSP00000478688.1:n.560-2144C>A
NM_000488.3:c.1068C>A , LRG_577t1:c.1068C>A	NP_000479.1:p.Arg356=
XM_005245198.2:c.924C>A	XP_005245255.1:p.Arg308=
NM_001365052.1:c.924C>A	NP_001351981.1:p.Arg308=
NM_000488.4:c.1068C>A MANE Select	NP_000479.1:p.Arg356=
NM_001365052.2:c.924C>A	NP_001351981.1:p.Arg308=
NM_001386302.1:c.1191C>A	NP_001373231.1:p.Arg397=
NM_001386303.1:c.1149C>A	NP_001373232.1:p.Arg383=
NM_001386304.1:c.1047C>A	NP_001373233.1:p.Arg349=
NM_001386305.1:c.1011C>A	NP_001373234.1:p.Arg337=
NM_001386306.1:c.852C>A	NP_001373235.1:p.Arg284=