Canonical Allele Identifier: CA343774597

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173879006A>T (hg19) ; chr1:g.173909868A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909868A>T , CM000663.2:g.173909868A>T	GRCh38
NC_000001.10:g.173879006A>T , CM000663.1:g.173879006A>T	GRCh37
NC_000001.9:g.172145629A>T	NCBI36
NG_012462.1:g.12511T>A , LRG_577:g.12511T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.837T>A MANE Select	ENSP00000356671.3:p.Cys279Ter
ENST00000367698.3:c.837T>A	ENSP00000356671.3:p.Cys279Ter
ENST00000487183.1:n.488T>A
ENST00000617423.4:c.559+1996T>A	ENSP00000478688.1:n.559+1996T>A
NM_000488.3:c.837T>A , LRG_577t1:c.837T>A	NP_000479.1:p.Cys279Ter
XM_005245198.2:c.693T>A	XP_005245255.1:p.Cys231Ter
NM_001365052.1:c.693T>A	NP_001351981.1:p.Cys231Ter
NM_000488.4:c.837T>A MANE Select	NP_000479.1:p.Cys279Ter
NM_001365052.2:c.693T>A	NP_001351981.1:p.Cys231Ter
NM_001386302.1:c.960T>A	NP_001373231.1:p.Cys320Ter
NM_001386303.1:c.918T>A	NP_001373232.1:p.Cys306Ter
NM_001386304.1:c.816T>A	NP_001373233.1:p.Cys272Ter
NM_001386305.1:c.780T>A	NP_001373234.1:p.Cys260Ter
NM_001386306.1:c.621T>A	NP_001373235.1:p.Cys207Ter