Canonical Allele Identifier: CA32782336

Gene: SERPINC1

Linked Data

• dbSNP Id: rs892676309
• MyVariant Identifiers: chr1:g.173883973G>A (hg19) ; chr1:g.173914835G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914835G>A , CM000663.2:g.173914835G>A	GRCh38
NC_000001.10:g.173883973G>A , CM000663.1:g.173883973G>A	GRCh37
NC_000001.9:g.172150596G>A	NCBI36
NG_012462.1:g.7544C>T , LRG_577:g.7544C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.126C>T MANE Select	ENSP00000356671.3:p.Ala42=
ENST00000367698.3:c.126C>T	ENSP00000356671.3:p.Ala42=
ENST00000494024.1:n.352C>T
ENST00000617423.4:c.126C>T	ENSP00000478688.1:p.Ala42=
NM_000488.3:c.126C>T , LRG_577t1:c.126C>T	NP_000479.1:p.Ala42=
XM_005245198.2:c.-19C>T	XP_005245255.1:n.-19C>T
NM_001365052.1:c.-19C>T	NP_001351981.1:n.-19C>T
NM_000488.4:c.126C>T MANE Select	NP_000479.1:p.Ala42=
NM_001365052.2:c.-19C>T	NP_001351981.1:n.-19C>T
NM_001386302.1:c.126C>T	NP_001373231.1:p.Ala42=
NM_001386303.1:c.207C>T	NP_001373232.1:p.Ala69=
NM_001386304.1:c.126C>T	NP_001373233.1:p.Ala42=
NM_001386305.1:c.126C>T	NP_001373234.1:p.Ala42=
NM_001386306.1:c.126C>T	NP_001373235.1:p.Ala42=