Canonical Allele Identifier: CA2578563064

Gene: VARS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30923509A>C , CM000668.2:g.30923509A>C	GRCh38
NC_000006.11:g.30891286A>C , CM000668.1:g.30891286A>C	GRCh37
NC_000006.10:g.30999265A>C	NCBI36
NG_034224.1:g.14302A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541562.6:c.2466+4A>C	ENSP00000441000.2:n.2466+4A>C
ENST00000672801.1:c.2460+4A>C	ENSP00000500615.1:n.2460+4A>C
ENST00000676266.1:c.2466+4A>C MANE Select	ENSP00000502585.1:n.2466+4A>C
ENST00000321897.9:c.2466+4A>C	ENSP00000316092.5:n.2466+4A>C
ENST00000469358.5:n.2454+4A>C
ENST00000473916.1:n.181A>C
ENST00000476162.5:n.1253+4A>C
ENST00000477288.5:n.5079+4A>C
ENST00000541562.5:c.2556+4A>C	ENSP00000441000.1:n.2556+4A>C
ENST00000542001.5:c.2460+4A>C	ENSP00000438200.2:n.2460+4A>C
ENST00000625423.2:c.2046+4A>C	ENSP00000485818.1:n.2046+4A>C
NM_001167733.2:c.2046+4A>C	NP_001161205.1:n.2046+4A>C
NM_001167734.1:c.2556+4A>C	NP_001161206.1:n.2556+4A>C
NM_020442.5:c.2466+4A>C	NP_065175.4:n.2466+4A>C
NM_001167733.3:c.2046+4A>C	NP_001161205.1:n.2046+4A>C
NM_001167734.2:c.2556+4A>C	NP_001161206.1:n.2556+4A>C
NM_020442.6:c.2466+4A>C MANE Select	NP_065175.4:n.2466+4A>C