Canonical Allele Identifier: CA2612686727

Gene: OTOG

Linked Data

• gnomAD v4: 11-17612559-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612559C>T , CM000673.2:g.17612559C>T	GRCh38
NC_000011.9:g.17634106C>T , CM000673.1:g.17634106C>T	GRCh37
NC_000011.8:g.17590682C>T	NCBI36
NG_033191.1:g.70187C>T
NG_033191.2:g.70187C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000399391.7:c.6329-61C>T	ENSP00000382323.2:n.6329-61C>T
ENST00000399397.6:c.6293-61C>T MANE Select	ENSP00000382329.2:n.6293-61C>T
ENST00000342528.2:c.3347-61C>T	ENSP00000341666.2:n.3347-61C>T
ENST00000399391.6:c.6329-61C>T	ENSP00000382323.2:n.6329-61C>T
ENST00000399397.5:c.6293-61C>T	ENSP00000382329.2:n.6293-61C>T
NM_001277269.1:c.6329-61C>T	NP_001264198.1:n.6329-61C>T
NM_001292063.1:c.6293-61C>T	NP_001278992.1:n.6293-61C>T
NM_001277269.2:c.6329-61C>T	NP_001264198.1:n.6329-61C>T
NM_001292063.2:c.6293-61C>T MANE Select	NP_001278992.1:n.6293-61C>T