Canonical Allele Identifier: CA385850039

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80632657T>G (hg19) ; chr12:g.80238877T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80238877T>G , CM000674.2:g.80238877T>G	GRCh38
NC_000012.11:g.80632657T>G , CM000674.1:g.80632657T>G	GRCh37
NC_000012.10:g.79156788T>G	NCBI36
NG_033008.1:g.34425T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000547103.7:c.844T>G MANE Select	ENSP00000447211.2:p.Phe282Val
ENST00000643417.1:n.1504T>G
ENST00000646859.1:c.844T>G	ENSP00000496036.1:p.Phe282Val
ENST00000458043.6:c.817T>G	ENSP00000400895.2:p.Phe273Val
ENST00000547103.5:c.817T>G	ENSP00000447211.1:p.Phe273Val
NM_173591.3:c.817T>G	NP_775862.3:p.Phe273Val
XM_005268802.2:c.868T>G	XP_005268859.1:p.Phe290Val
XM_011538191.1:c.868T>G	XP_011536493.1:p.Phe290Val
XM_011538192.1:c.715T>G	XP_011536494.1:p.Phe239Val
XM_011538193.1:c.502T>G	XP_011536495.1:p.Phe168Val
XM_005268802.3:c.868T>G	XP_005268859.1:p.Phe290Val
XM_011538192.2:c.715T>G	XP_011536494.1:p.Phe239Val
NM_001368062.1:c.817T>G	NP_001354991.1:p.Phe273Val
NM_001368062.3:c.844T>G	NP_001354991.2:p.Phe282Val
NM_001378609.3:c.844T>G MANE Select	NP_001365538.2:p.Phe282Val
NM_001378610.3:c.844T>G	NP_001365539.2:p.Phe282Val
NM_173591.7:c.844T>G	NP_775862.4:p.Phe282Val