Canonical Allele Identifier: CA343772656

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873184T>A (hg19) ; chr1:g.173904046T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904046T>A , CM000663.2:g.173904046T>A	GRCh38
NC_000001.10:g.173873184T>A , CM000663.1:g.173873184T>A	GRCh37
NC_000001.9:g.172139807T>A	NCBI36
NG_012462.1:g.18333A>T , LRG_577:g.18333A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1238A>T MANE Select	ENSP00000356671.3:p.Glu413Val
ENST00000367698.3:c.1238A>T	ENSP00000356671.3:p.Glu413Val
ENST00000617423.4:c.623A>T	ENSP00000478688.1:p.Glu208Val
NM_000488.3:c.1238A>T , LRG_577t1:c.1238A>T	NP_000479.1:p.Glu413Val
XM_005245198.2:c.1094A>T	XP_005245255.1:p.Glu365Val
NM_001365052.1:c.1094A>T	NP_001351981.1:p.Glu365Val
NM_000488.4:c.1238A>T MANE Select	NP_000479.1:p.Glu413Val
NM_001365052.2:c.1094A>T	NP_001351981.1:p.Glu365Val
NM_001386302.1:c.1361A>T	NP_001373231.1:p.Glu454Val
NM_001386303.1:c.1319A>T	NP_001373232.1:p.Glu440Val
NM_001386304.1:c.1217A>T	NP_001373233.1:p.Glu406Val
NM_001386305.1:c.1181A>T	NP_001373234.1:p.Glu394Val
NM_001386306.1:c.1022A>T	NP_001373235.1:p.Glu341Val