Canonical Allele Identifier: CA1618928555

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923376T= , CM000668.2:g.30923376T=	GRCh38
NC_000006.11:g.30891153T= , CM000668.1:g.30891153T=	GRCh37
NC_000006.10:g.30999132T=	NCBI36
NG_034224.1:g.14169T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2337T=	ENSP00000441000.2:p.Asp779=
ENST00000672801.1:c.2331T=	ENSP00000500615.1:p.Asp777=
ENST00000676266.1:c.2337T= MANE Select	ENSP00000502585.1:p.Asp779=
ENST00000321897.9:c.2337T=	ENSP00000316092.5:p.Asp779=
ENST00000469358.5:n.2325T=
ENST00000473916.1:n.48T=
ENST00000476162.5:n.1124T=
ENST00000477052.1:n.423T=
ENST00000477288.5:n.4950T=
ENST00000541562.5:c.2427T=	ENSP00000441000.1:p.Asp809=
ENST00000542001.5:c.2331T=	ENSP00000438200.2:p.Asp777=
ENST00000625423.2:c.1917T=	ENSP00000485818.1:p.Asp639=
NM_001167733.2:c.1917T=	NP_001161205.1:p.Asp639=
NM_001167734.1:c.2427T=	NP_001161206.1:p.Asp809=
NM_020442.5:c.2337T=	NP_065175.4:p.Asp779=
NM_001167733.3:c.1917T=	NP_001161205.1:p.Asp639=
NM_001167734.2:c.2427T=	NP_001161206.1:p.Asp809=
NM_020442.6:c.2337T= MANE Select	NP_065175.4:p.Asp779=