Canonical Allele Identifier: CA385888721

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752482A>T (hg19) ; chr12:g.80358702A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358702A>T , CM000674.2:g.80358702A>T	GRCh38
NC_000012.11:g.80752482A>T , CM000674.1:g.80752482A>T	GRCh37
NC_000012.10:g.79276613A>T	NCBI36
NG_033008.1:g.154250A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6153A>T MANE Select	ENSP00000447211.2:p.Leu2051Phe
ENST00000642294.1:c.93A>T	ENSP00000493572.1:p.Leu31Phe
ENST00000646859.1:c.6018A>T	ENSP00000496036.1:p.Leu2006Phe
ENST00000298820.7:c.1454A>T
ENST00000458043.6:c.6126A>T	ENSP00000400895.2:p.Leu2042Phe
ENST00000546620.5:n.409A>T
ENST00000547103.5:c.6090A>T	ENSP00000447211.1:p.Leu2030Phe
ENST00000550182.2:c.177A>T	ENSP00000449641.1:p.Leu59Phe
ENST00000551340.5:c.281A>T
NM_173591.3:c.6126A>T	NP_775862.3:p.Leu2042Phe
XM_005268802.2:c.6177A>T	XP_005268859.1:p.Leu2059Phe
XM_011538191.1:c.6177A>T	XP_011536493.1:p.Leu2059Phe
XM_011538192.1:c.6024A>T	XP_011536494.1:p.Leu2008Phe
XM_011538193.1:c.5811A>T	XP_011536495.1:p.Leu1937Phe
XM_005268802.3:c.6177A>T	XP_005268859.1:p.Leu2059Phe
XM_011538192.2:c.6024A>T	XP_011536494.1:p.Leu2008Phe
NM_001368062.1:c.5991A>T	NP_001354991.1:p.Leu1997Phe
NM_001368062.3:c.6018A>T	NP_001354991.2:p.Leu2006Phe
NM_001378609.3:c.6153A>T MANE Select	NP_001365538.2:p.Leu2051Phe
NM_001378610.3:c.6153A>T	NP_001365539.2:p.Leu2051Phe
NM_173591.7:c.6153A>T	NP_775862.4:p.Leu2051Phe