Canonical Allele Identifier: CA385888833

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752531C>G (hg19) ; chr12:g.80358751C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358751C>G , CM000674.2:g.80358751C>G	GRCh38
NC_000012.11:g.80752531C>G , CM000674.1:g.80752531C>G	GRCh37
NC_000012.10:g.79276662C>G	NCBI36
NG_033008.1:g.154299C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6202C>G MANE Select	ENSP00000447211.2:p.Gln2068Glu
ENST00000642294.1:c.142C>G	ENSP00000493572.1:p.Gln48Glu
ENST00000646859.1:c.6067C>G	ENSP00000496036.1:p.Gln2023Glu
ENST00000298820.7:c.1503C>G
ENST00000458043.6:c.6175C>G	ENSP00000400895.2:p.Gln2059Glu
ENST00000546620.5:n.458C>G
ENST00000547103.5:c.6139C>G	ENSP00000447211.1:p.Gln2047Glu
ENST00000550182.2:c.226C>G	ENSP00000449641.1:p.Gln76Glu
ENST00000551340.5:c.330C>G
NM_173591.3:c.6175C>G	NP_775862.3:p.Gln2059Glu
XM_005268802.2:c.6226C>G	XP_005268859.1:p.Gln2076Glu
XM_011538191.1:c.6226C>G	XP_011536493.1:p.Gln2076Glu
XM_011538192.1:c.6073C>G	XP_011536494.1:p.Gln2025Glu
XM_011538193.1:c.5860C>G	XP_011536495.1:p.Gln1954Glu
XM_005268802.3:c.6226C>G	XP_005268859.1:p.Gln2076Glu
XM_011538192.2:c.6073C>G	XP_011536494.1:p.Gln2025Glu
NM_001368062.1:c.6040C>G	NP_001354991.1:p.Gln2014Glu
NM_001368062.3:c.6067C>G	NP_001354991.2:p.Gln2023Glu
NM_001378609.3:c.6202C>G MANE Select	NP_001365538.2:p.Gln2068Glu
NM_001378610.3:c.6202C>G	NP_001365539.2:p.Gln2068Glu
NM_173591.7:c.6202C>G	NP_775862.4:p.Gln2068Glu