Canonical Allele Identifier: CA2978195047

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80266358A>T , CM000674.2:g.80266358A>T	GRCh38
NC_000012.11:g.80660138A>T , CM000674.1:g.80660138A>T	GRCh37
NC_000012.10:g.79184269A>T	NCBI36
NG_033008.1:g.61906A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378609.3:c.2225-93A>T MANE Select	NP_001365538.2:n.2225-93A>T
ENST00000547103.7:c.2225-93A>T MANE Select	ENSP00000447211.2:n.2225-93A>T
NM_001368062.1:c.2198-93A>T	NP_001354991.1:n.2198-93A>T
NM_001368062.3:c.2225-93A>T	NP_001354991.2:n.2225-93A>T
NM_001378610.3:c.2225-93A>T	NP_001365539.2:n.2225-93A>T
NM_173591.3:c.2198-93A>T	NP_775862.3:n.2198-93A>T
NM_173591.7:c.2225-93A>T	NP_775862.4:n.2225-93A>T
ENST00000458043.6:c.2198-93A>T	ENSP00000400895.2:n.2198-93A>T
ENST00000547103.5:c.2198-93A>T	ENSP00000447211.1:n.2198-93A>T
ENST00000646859.1:c.2225-93A>T	ENSP00000496036.1:n.2225-93A>T
XM_005268802.2:c.2249-93A>T	XP_005268859.1:n.2249-93A>T
XM_005268802.3:c.2249-93A>T	XP_005268859.1:n.2249-93A>T
XM_011538191.1:c.2249-93A>T	XP_011536493.1:n.2249-93A>T
XM_011538192.1:c.2096-93A>T	XP_011536494.1:n.2096-93A>T
XM_011538192.2:c.2096-93A>T	XP_011536494.1:n.2096-93A>T
XM_011538193.1:c.1883-93A>T	XP_011536495.1:n.1883-93A>T