Canonical Allele Identifier: CA379811368

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17574961G>T (hg19) ; chr11:g.17553414G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553414G>T , CM000673.2:g.17553414G>T	GRCh38
NC_000011.9:g.17574961G>T , CM000673.1:g.17574961G>T	GRCh37
NC_000011.8:g.17531537G>T	NCBI36
NG_033191.1:g.11042G>T
NG_033191.2:g.11042G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.471G>T	ENSP00000382323.2:p.Gln157His
ENST00000399397.6:c.435G>T MANE Select	ENSP00000382329.2:p.Gln145His
ENST00000399391.6:c.471G>T	ENSP00000382323.2:p.Gln157His
ENST00000399397.5:c.435G>T	ENSP00000382329.2:p.Gln145His
ENST00000428619.1:c.252G>T	ENSP00000399057.2:p.Gln84His
ENST00000498332.5:n.341G>T
NM_001277269.1:c.471G>T	NP_001264198.1:p.Gln157His
NM_001292063.1:c.435G>T	NP_001278992.1:p.Gln145His
NM_001277269.2:c.471G>T	NP_001264198.1:p.Gln157His
NM_001292063.2:c.435G>T MANE Select	NP_001278992.1:p.Gln145His