Canonical Allele Identifier: CA421942687

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173884036C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914898C>T , CM000663.2:g.173914898C>T	GRCh38
NC_000001.10:g.173884036C>T , CM000663.1:g.173884036C>T	GRCh37
NC_000001.9:g.172150659C>T	NCBI36
NG_012462.1:g.7481G>A , LRG_577:g.7481G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.63G>A MANE Select	ENSP00000356671.3:p.Leu21=
ENST00000367698.3:c.63G>A	ENSP00000356671.3:p.Leu21=
ENST00000494024.1:n.289G>A
ENST00000617423.4:c.63G>A	ENSP00000478688.1:p.Leu21=
NM_000488.3:c.63G>A , LRG_577t1:c.63G>A	NP_000479.1:p.Leu21=
XM_005245198.2:c.-82G>A	XP_005245255.1:n.-82G>A
NM_001365052.1:c.-82G>A	NP_001351981.1:n.-82G>A
NM_000488.4:c.63G>A MANE Select	NP_000479.1:p.Leu21=
NM_001365052.2:c.-82G>A	NP_001351981.1:n.-82G>A
NM_001386302.1:c.63G>A	NP_001373231.1:p.Leu21=
NM_001386303.1:c.144G>A	NP_001373232.1:p.Leu48=
NM_001386304.1:c.63G>A	NP_001373233.1:p.Leu21=
NM_001386305.1:c.63G>A	NP_001373234.1:p.Leu21=
NM_001386306.1:c.63G>A	NP_001373235.1:p.Leu21=