Canonical Allele Identifier: CA343777758

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173883842G>T (hg19) ; chr1:g.173914704G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914704G>T , CM000663.2:g.173914704G>T	GRCh38
NC_000001.10:g.173883842G>T , CM000663.1:g.173883842G>T	GRCh37
NC_000001.9:g.172150465G>T	NCBI36
NG_012462.1:g.7675C>A , LRG_577:g.7675C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.257C>A MANE Select	ENSP00000356671.3:p.Ala86Asp
ENST00000367698.3:c.257C>A	ENSP00000356671.3:p.Ala86Asp
ENST00000494024.1:n.483C>A
ENST00000617423.4:c.257C>A	ENSP00000478688.1:p.Ala86Asp
NM_000488.3:c.257C>A , LRG_577t1:c.257C>A	NP_000479.1:p.Ala86Asp
XM_005245198.2:c.113C>A	XP_005245255.1:p.Ala38Asp
NM_001365052.1:c.113C>A	NP_001351981.1:p.Ala38Asp
NM_000488.4:c.257C>A MANE Select	NP_000479.1:p.Ala86Asp
NM_001365052.2:c.113C>A	NP_001351981.1:p.Ala38Asp
NM_001386302.1:c.257C>A	NP_001373231.1:p.Ala86Asp
NM_001386303.1:c.338C>A	NP_001373232.1:p.Ala113Asp
NM_001386304.1:c.257C>A	NP_001373233.1:p.Ala86Asp
NM_001386305.1:c.257C>A	NP_001373234.1:p.Ala86Asp
NM_001386306.1:c.257C>A	NP_001373235.1:p.Ala86Asp