Canonical Allele Identifier: CA2620017217
Gene: OTOGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80359049_80359050insCTG , CM000674.2:g.80359049_80359050insCTG GRCh38
NC_000012.11:g.80752829_80752830insCTG , CM000674.1:g.80752829_80752830insCTG GRCh37
NC_000012.10:g.79276960_79276961insCTG NCBI36
NG_033008.1:g.154597_154598insCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000547103.7:c.6267+149_6267+150insCTG MANE Select ENSP00000447211.2:n.6267+149_6267+150insCTG
ENST00000642294.1:c.207+149_207+150insCTG ENSP00000493572.1:n.207+149_207+150insCTG
ENST00000646859.1:c.6132+149_6132+150insCTG ENSP00000496036.1:n.6132+149_6132+150insCTG
ENST00000298820.7:c.1527+274_1527+275insCTG
ENST00000458043.6:c.6240+149_6240+150insCTG ENSP00000400895.2:n.6240+149_6240+150insCTG
ENST00000546620.5:n.523+149_523+150insCTG
ENST00000547103.5:c.6204+149_6204+150insCTG ENSP00000447211.1:n.6204+149_6204+150insCTG
ENST00000550182.2:c.291+149_291+150insCTG ENSP00000449641.1:n.291+149_291+150insCTG
ENST00000551340.5:c.395+149_395+150insCTG
NM_173591.3:c.6240+149_6240+150insCTG NP_775862.3:n.6240+149_6240+150insCTG
XM_005268802.2:c.6291+149_6291+150insCTG XP_005268859.1:n.6291+149_6291+150insCTG
XM_011538191.1:c.6291+149_6291+150insCTG XP_011536493.1:n.6291+149_6291+150insCTG
XM_011538192.1:c.6138+149_6138+150insCTG XP_011536494.1:n.6138+149_6138+150insCTG
XM_011538193.1:c.5925+149_5925+150insCTG XP_011536495.1:n.5925+149_5925+150insCTG
XM_005268802.3:c.6291+149_6291+150insCTG XP_005268859.1:n.6291+149_6291+150insCTG
XM_011538192.2:c.6138+149_6138+150insCTG XP_011536494.1:n.6138+149_6138+150insCTG
NM_001368062.1:c.6105+149_6105+150insCTG NP_001354991.1:n.6105+149_6105+150insCTG
NM_001368062.3:c.6132+149_6132+150insCTG NP_001354991.2:n.6132+149_6132+150insCTG
NM_001378609.3:c.6267+149_6267+150insCTG MANE Select NP_001365538.2:n.6267+149_6267+150insCTG
NM_001378610.3:c.6267+149_6267+150insCTG NP_001365539.2:n.6267+149_6267+150insCTG
NM_173591.7:c.6267+149_6267+150insCTG NP_775862.4:n.6267+149_6267+150insCTG