Canonical Allele Identifier: CA1618928389

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922989G= , CM000668.2:g.30922989G=	GRCh38
NC_000006.11:g.30890766G= , CM000668.1:g.30890766G=	GRCh37
NC_000006.10:g.30998745G=	NCBI36
NG_034224.1:g.13782G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2185+13G=	ENSP00000441000.2:n.2185+13G=
ENST00000672801.1:c.2179+13G=	ENSP00000500615.1:n.2179+13G=
ENST00000676266.1:c.2185+13G= MANE Select	ENSP00000502585.1:n.2185+13G=
ENST00000321897.9:c.2185+13G=	ENSP00000316092.5:n.2185+13G=
ENST00000469358.5:n.2173+13G=
ENST00000476162.5:n.972+13G=
ENST00000477052.1:n.271+13G=
ENST00000477288.5:n.4798+13G=
ENST00000541562.5:c.2275+13G=	ENSP00000441000.1:n.2275+13G=
ENST00000542001.5:c.2179+13G=	ENSP00000438200.2:n.2179+13G=
ENST00000625423.2:c.1765+13G=	ENSP00000485818.1:n.1765+13G=
NM_001167733.2:c.1765+13G=	NP_001161205.1:n.1765+13G=
NM_001167734.1:c.2275+13G=	NP_001161206.1:n.2275+13G=
NM_020442.5:c.2185+13G=	NP_065175.4:n.2185+13G=
NM_001167733.3:c.1765+13G=	NP_001161205.1:n.1765+13G=
NM_001167734.2:c.2275+13G=	NP_001161206.1:n.2275+13G=
NM_020442.6:c.2185+13G= MANE Select	NP_065175.4:n.2185+13G=