Canonical Allele Identifier: CA2620017115

Gene: OTOGL

Linked Data

• gnomAD v4: 12-80358829-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358829C>T , CM000674.2:g.80358829C>T	GRCh38
NC_000012.11:g.80752609C>T , CM000674.1:g.80752609C>T	GRCh37
NC_000012.10:g.79276740C>T	NCBI36
NG_033008.1:g.154377C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6227-31C>T MANE Select	ENSP00000447211.2:n.6227-31C>T
ENST00000642294.1:c.167-31C>T	ENSP00000493572.1:n.167-31C>T
ENST00000646859.1:c.6092-31C>T	ENSP00000496036.1:n.6092-31C>T
ENST00000298820.7:c.1527+54C>T
ENST00000458043.6:c.6200-31C>T	ENSP00000400895.2:n.6200-31C>T
ENST00000546620.5:n.483-31C>T
ENST00000547103.5:c.6164-31C>T	ENSP00000447211.1:n.6164-31C>T
ENST00000550182.2:c.251-31C>T	ENSP00000449641.1:n.251-31C>T
ENST00000551340.5:c.355-31C>T
NM_173591.3:c.6200-31C>T	NP_775862.3:n.6200-31C>T
XM_005268802.2:c.6251-31C>T	XP_005268859.1:n.6251-31C>T
XM_011538191.1:c.6251-31C>T	XP_011536493.1:n.6251-31C>T
XM_011538192.1:c.6098-31C>T	XP_011536494.1:n.6098-31C>T
XM_011538193.1:c.5885-31C>T	XP_011536495.1:n.5885-31C>T
XM_005268802.3:c.6251-31C>T	XP_005268859.1:n.6251-31C>T
XM_011538192.2:c.6098-31C>T	XP_011536494.1:n.6098-31C>T
NM_001368062.1:c.6065-31C>T	NP_001354991.1:n.6065-31C>T
NM_001368062.3:c.6092-31C>T	NP_001354991.2:n.6092-31C>T
NM_001378609.3:c.6227-31C>T MANE Select	NP_001365538.2:n.6227-31C>T
NM_001378610.3:c.6227-31C>T	NP_001365539.2:n.6227-31C>T
NM_173591.7:c.6227-31C>T	NP_775862.4:n.6227-31C>T