Canonical Allele Identifier: CA2574770896

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612581G>C , CM000673.2:g.17612581G>C	GRCh38
NC_000011.9:g.17634128G>C , CM000673.1:g.17634128G>C	GRCh37
NC_000011.8:g.17590704G>C	NCBI36
NG_033191.1:g.70209G>C
NG_033191.2:g.70209G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6329-39G>C	ENSP00000382323.2:n.6329-39G>C
ENST00000399397.6:c.6293-39G>C MANE Select	ENSP00000382329.2:n.6293-39G>C
ENST00000342528.2:c.3347-39G>C	ENSP00000341666.2:n.3347-39G>C
ENST00000399391.6:c.6329-39G>C	ENSP00000382323.2:n.6329-39G>C
ENST00000399397.5:c.6293-39G>C	ENSP00000382329.2:n.6293-39G>C
NM_001277269.1:c.6329-39G>C	NP_001264198.1:n.6329-39G>C
NM_001292063.1:c.6293-39G>C	NP_001278992.1:n.6293-39G>C
NM_001277269.2:c.6329-39G>C	NP_001264198.1:n.6329-39G>C
NM_001292063.2:c.6293-39G>C MANE Select	NP_001278992.1:n.6293-39G>C