Canonical Allele Identifier: CA473305717

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17634186T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612639T>G , CM000673.2:g.17612639T>G	GRCh38
NC_000011.9:g.17634186T>G , CM000673.1:g.17634186T>G	GRCh37
NC_000011.8:g.17590762T>G	NCBI36
NG_033191.1:g.70267T>G
NG_033191.2:g.70267T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6348T>G	ENSP00000382323.2:p.Pro2116=
ENST00000399397.6:c.6312T>G MANE Select	ENSP00000382329.2:p.Pro2104=
ENST00000342528.2:c.3366T>G	ENSP00000341666.2:p.Pro1122=
ENST00000399391.6:c.6348T>G	ENSP00000382323.2:p.Pro2116=
ENST00000399397.5:c.6312T>G	ENSP00000382329.2:p.Pro2104=
NM_001277269.1:c.6348T>G	NP_001264198.1:p.Pro2116=
NM_001292063.1:c.6312T>G	NP_001278992.1:p.Pro2104=
NM_001277269.2:c.6348T>G	NP_001264198.1:p.Pro2116=
NM_001292063.2:c.6312T>G MANE Select	NP_001278992.1:p.Pro2104=