Canonical Allele Identifier: CA473301206

Gene: OTOG

Linked Data

• gnomAD v4: 11-17645848-G-T
• MyVariant Identifiers: chr11:g.17667395G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17645848G>T , CM000673.2:g.17645848G>T	GRCh38
NC_000011.9:g.17667395G>T , CM000673.1:g.17667395G>T	GRCh37
NC_000011.8:g.17623971G>T	NCBI36
NG_033191.1:g.103476G>T
NG_033191.2:g.103476G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399391.7:c.8682G>T	ENSP00000382323.2:p.Leu2894=
ENST00000399397.6:c.8646G>T MANE Select	ENSP00000382329.2:p.Leu2882=
ENST00000399391.6:c.8682G>T	ENSP00000382323.2:p.Leu2894=
ENST00000399397.5:c.8646G>T	ENSP00000382329.2:p.Leu2882=
NM_001277269.1:c.8682G>T	NP_001264198.1:p.Leu2894=
NM_001292063.1:c.8646G>T	NP_001278992.1:p.Leu2882=
NM_001277269.2:c.8682G>T	NP_001264198.1:p.Leu2894=
NM_001292063.2:c.8646G>T MANE Select	NP_001278992.1:p.Leu2882=