Canonical Allele Identifier: CA343772684

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873195T>A (hg19) ; chr1:g.173904057T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904057T>A , CM000663.2:g.173904057T>A	GRCh38
NC_000001.10:g.173873195T>A , CM000663.1:g.173873195T>A	GRCh37
NC_000001.9:g.172139818T>A	NCBI36
NG_012462.1:g.18322A>T , LRG_577:g.18322A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1227A>T MANE Select	ENSP00000356671.3:p.Glu409Asp
ENST00000367698.3:c.1227A>T	ENSP00000356671.3:p.Glu409Asp
ENST00000617423.4:c.612A>T	ENSP00000478688.1:p.Glu204Asp
NM_000488.3:c.1227A>T , LRG_577t1:c.1227A>T	NP_000479.1:p.Glu409Asp
XM_005245198.2:c.1083A>T	XP_005245255.1:p.Glu361Asp
NM_001365052.1:c.1083A>T	NP_001351981.1:p.Glu361Asp
NM_000488.4:c.1227A>T MANE Select	NP_000479.1:p.Glu409Asp
NM_001365052.2:c.1083A>T	NP_001351981.1:p.Glu361Asp
NM_001386302.1:c.1350A>T	NP_001373231.1:p.Glu450Asp
NM_001386303.1:c.1308A>T	NP_001373232.1:p.Glu436Asp
NM_001386304.1:c.1206A>T	NP_001373233.1:p.Glu402Asp
NM_001386305.1:c.1170A>T	NP_001373234.1:p.Glu390Asp
NM_001386306.1:c.1011A>T	NP_001373235.1:p.Glu337Asp