Canonical Allele Identifier: CA1618928596

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923456C= , CM000668.2:g.30923456C=	GRCh38
NC_000006.11:g.30891233C= , CM000668.1:g.30891233C=	GRCh37
NC_000006.10:g.30999212C=	NCBI36
NG_034224.1:g.14249C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2417C=	ENSP00000441000.2:p.Thr806=
ENST00000672801.1:c.2411C=	ENSP00000500615.1:p.Thr804=
ENST00000676266.1:c.2417C= MANE Select	ENSP00000502585.1:p.Thr806=
ENST00000321897.9:c.2417C=	ENSP00000316092.5:p.Thr806=
ENST00000469358.5:n.2405C=
ENST00000473916.1:n.128C=
ENST00000476162.5:n.1204C=
ENST00000477052.1:n.503C=
ENST00000477288.5:n.5030C=
ENST00000541562.5:c.2507C=	ENSP00000441000.1:p.Thr836=
ENST00000542001.5:c.2411C=	ENSP00000438200.2:p.Thr804=
ENST00000625423.2:c.1997C=	ENSP00000485818.1:p.Thr666=
NM_001167733.2:c.1997C=	NP_001161205.1:p.Thr666=
NM_001167734.1:c.2507C=	NP_001161206.1:p.Thr836=
NM_020442.5:c.2417C=	NP_065175.4:p.Thr806=
NM_001167733.3:c.1997C=	NP_001161205.1:p.Thr666=
NM_001167734.2:c.2507C=	NP_001161206.1:p.Thr836=
NM_020442.6:c.2417C= MANE Select	NP_065175.4:p.Thr806=