Canonical Allele Identifier: CA2620011012

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80266344C>A , CM000674.2:g.80266344C>A	GRCh38
NC_000012.11:g.80660124C>A , CM000674.1:g.80660124C>A	GRCh37
NC_000012.10:g.79184255C>A	NCBI36
NG_033008.1:g.61892C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378609.3:c.2225-107C>A MANE Select	NP_001365538.2:n.2225-107C>A
ENST00000547103.7:c.2225-107C>A MANE Select	ENSP00000447211.2:n.2225-107C>A
NM_001368062.1:c.2198-107C>A	NP_001354991.1:n.2198-107C>A
NM_001368062.3:c.2225-107C>A	NP_001354991.2:n.2225-107C>A
NM_001378610.3:c.2225-107C>A	NP_001365539.2:n.2225-107C>A
NM_173591.3:c.2198-107C>A	NP_775862.3:n.2198-107C>A
NM_173591.7:c.2225-107C>A	NP_775862.4:n.2225-107C>A
ENST00000458043.6:c.2198-107C>A	ENSP00000400895.2:n.2198-107C>A
ENST00000547103.5:c.2198-107C>A	ENSP00000447211.1:n.2198-107C>A
ENST00000646859.1:c.2225-107C>A	ENSP00000496036.1:n.2225-107C>A
XM_005268802.2:c.2249-107C>A	XP_005268859.1:n.2249-107C>A
XM_005268802.3:c.2249-107C>A	XP_005268859.1:n.2249-107C>A
XM_011538191.1:c.2249-107C>A	XP_011536493.1:n.2249-107C>A
XM_011538192.1:c.2096-107C>A	XP_011536494.1:n.2096-107C>A
XM_011538192.2:c.2096-107C>A	XP_011536494.1:n.2096-107C>A
XM_011538193.1:c.1883-107C>A	XP_011536495.1:n.1883-107C>A