Canonical Allele Identifier: CA343774826

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173879079C>T (hg19) ; chr1:g.173909941C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909941C>T , CM000663.2:g.173909941C>T	GRCh38
NC_000001.10:g.173879079C>T , CM000663.1:g.173879079C>T	GRCh37
NC_000001.9:g.172145702C>T	NCBI36
NG_012462.1:g.12438G>A , LRG_577:g.12438G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.764G>A MANE Select	ENSP00000356671.3:p.Gly255Asp
ENST00000367698.3:c.764G>A	ENSP00000356671.3:p.Gly255Asp
ENST00000487183.1:n.415G>A
ENST00000617423.4:c.559+1923G>A	ENSP00000478688.1:n.559+1923G>A
NM_000488.3:c.764G>A , LRG_577t1:c.764G>A	NP_000479.1:p.Gly255Asp
XM_005245198.2:c.620G>A	XP_005245255.1:p.Gly207Asp
NM_001365052.1:c.620G>A	NP_001351981.1:p.Gly207Asp
NM_000488.4:c.764G>A MANE Select	NP_000479.1:p.Gly255Asp
NM_001365052.2:c.620G>A	NP_001351981.1:p.Gly207Asp
NM_001386302.1:c.887G>A	NP_001373231.1:p.Gly296Asp
NM_001386303.1:c.845G>A	NP_001373232.1:p.Gly282Asp
NM_001386304.1:c.743G>A	NP_001373233.1:p.Gly248Asp
NM_001386305.1:c.763-56G>A	NP_001373234.1:n.763-56G>A
NM_001386306.1:c.548G>A	NP_001373235.1:p.Gly183Asp