Canonical Allele Identifier: CA385888605

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752117C>G (hg19) ; chr12:g.80358337C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358337C>G , CM000674.2:g.80358337C>G	GRCh38
NC_000012.11:g.80752117C>G , CM000674.1:g.80752117C>G	GRCh37
NC_000012.10:g.79276248C>G	NCBI36
NG_033008.1:g.153885C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6109C>G MANE Select	ENSP00000447211.2:p.Gln2037Glu
ENST00000642294.1:c.49C>G	ENSP00000493572.1:p.Gln17Glu
ENST00000646859.1:c.5974C>G	ENSP00000496036.1:p.Gln1992Glu
ENST00000298820.7:c.1410C>G
ENST00000458043.6:c.6082C>G	ENSP00000400895.2:p.Gln2028Glu
ENST00000546620.5:n.365C>G
ENST00000547103.5:c.6046C>G	ENSP00000447211.1:p.Gln2016Glu
ENST00000550182.2:c.133C>G	ENSP00000449641.1:p.Gln45Glu
ENST00000551340.5:c.237C>G
NM_173591.3:c.6082C>G	NP_775862.3:p.Gln2028Glu
XM_005268802.2:c.6133C>G	XP_005268859.1:p.Gln2045Glu
XM_011538191.1:c.6133C>G	XP_011536493.1:p.Gln2045Glu
XM_011538192.1:c.5980C>G	XP_011536494.1:p.Gln1994Glu
XM_011538193.1:c.5767C>G	XP_011536495.1:p.Gln1923Glu
XM_005268802.3:c.6133C>G	XP_005268859.1:p.Gln2045Glu
XM_011538192.2:c.5980C>G	XP_011536494.1:p.Gln1994Glu
NM_001368062.1:c.5947C>G	NP_001354991.1:p.Gln1983Glu
NM_001368062.3:c.5974C>G	NP_001354991.2:p.Gln1992Glu
NM_001378609.3:c.6109C>G MANE Select	NP_001365538.2:p.Gln2037Glu
NM_001378610.3:c.6109C>G	NP_001365539.2:p.Gln2037Glu
NM_173591.7:c.6109C>G	NP_775862.4:p.Gln2037Glu