Canonical Allele Identifier: CA343772701

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873202A>T (hg19) ; chr1:g.173904064A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904064A>T , CM000663.2:g.173904064A>T	GRCh38
NC_000001.10:g.173873202A>T , CM000663.1:g.173873202A>T	GRCh37
NC_000001.9:g.172139825A>T	NCBI36
NG_012462.1:g.18315T>A , LRG_577:g.18315T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1220T>A MANE Select	ENSP00000356671.3:p.Val407Glu
ENST00000367698.3:c.1220T>A	ENSP00000356671.3:p.Val407Glu
ENST00000617423.4:c.605T>A	ENSP00000478688.1:p.Val202Glu
NM_000488.3:c.1220T>A , LRG_577t1:c.1220T>A	NP_000479.1:p.Val407Glu
XM_005245198.2:c.1076T>A	XP_005245255.1:p.Val359Glu
NM_001365052.1:c.1076T>A	NP_001351981.1:p.Val359Glu
NM_000488.4:c.1220T>A MANE Select	NP_000479.1:p.Val407Glu
NM_001365052.2:c.1076T>A	NP_001351981.1:p.Val359Glu
NM_001386302.1:c.1343T>A	NP_001373231.1:p.Val448Glu
NM_001386303.1:c.1301T>A	NP_001373232.1:p.Val434Glu
NM_001386304.1:c.1199T>A	NP_001373233.1:p.Val400Glu
NM_001386305.1:c.1163T>A	NP_001373234.1:p.Val388Glu
NM_001386306.1:c.1004T>A	NP_001373235.1:p.Val335Glu