Canonical Allele Identifier: CA385888903

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752640A>T (hg19) ; chr12:g.80358860A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358860A>T , CM000674.2:g.80358860A>T	GRCh38
NC_000012.11:g.80752640A>T , CM000674.1:g.80752640A>T	GRCh37
NC_000012.10:g.79276771A>T	NCBI36
NG_033008.1:g.154408A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6227A>T MANE Select	ENSP00000447211.2:p.Glu2076Val
ENST00000642294.1:c.167A>T	ENSP00000493572.1:p.Glu56Val
ENST00000646859.1:c.6092A>T	ENSP00000496036.1:p.Glu2031Val
ENST00000298820.7:c.1527+85A>T
ENST00000458043.6:c.6200A>T	ENSP00000400895.2:p.Glu2067Val
ENST00000546620.5:n.483A>T
ENST00000547103.5:c.6164A>T	ENSP00000447211.1:p.Glu2055Val
ENST00000550182.2:c.251A>T	ENSP00000449641.1:p.Glu84Val
ENST00000551340.5:c.355A>T
NM_173591.3:c.6200A>T	NP_775862.3:p.Glu2067Val
XM_005268802.2:c.6251A>T	XP_005268859.1:p.Glu2084Val
XM_011538191.1:c.6251A>T	XP_011536493.1:p.Glu2084Val
XM_011538192.1:c.6098A>T	XP_011536494.1:p.Glu2033Val
XM_011538193.1:c.5885A>T	XP_011536495.1:p.Glu1962Val
XM_005268802.3:c.6251A>T	XP_005268859.1:p.Glu2084Val
XM_011538192.2:c.6098A>T	XP_011536494.1:p.Glu2033Val
NM_001368062.1:c.6065A>T	NP_001354991.1:p.Glu2022Val
NM_001368062.3:c.6092A>T	NP_001354991.2:p.Glu2031Val
NM_001378609.3:c.6227A>T MANE Select	NP_001365538.2:p.Glu2076Val
NM_001378610.3:c.6227A>T	NP_001365539.2:p.Glu2076Val
NM_173591.7:c.6227A>T	NP_775862.4:p.Glu2076Val