Canonical Allele Identifier: CA1618928380

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30922978T= , CM000668.2:g.30922978T=	GRCh38
NC_000006.11:g.30890755T= , CM000668.1:g.30890755T=	GRCh37
NC_000006.10:g.30998734T=	NCBI36
NG_034224.1:g.13771T=

Transcript Alleles

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