Canonical Allele Identifier: CA385888650

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752451T>G (hg19) ; chr12:g.80358671T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358671T>G , CM000674.2:g.80358671T>G	GRCh38
NC_000012.11:g.80752451T>G , CM000674.1:g.80752451T>G	GRCh37
NC_000012.10:g.79276582T>G	NCBI36
NG_033008.1:g.154219T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6122T>G MANE Select	ENSP00000447211.2:p.Val2041Gly
ENST00000642294.1:c.62T>G	ENSP00000493572.1:p.Val21Gly
ENST00000646859.1:c.5987T>G	ENSP00000496036.1:p.Val1996Gly
ENST00000298820.7:c.1423T>G
ENST00000458043.6:c.6095T>G	ENSP00000400895.2:p.Val2032Gly
ENST00000546620.5:n.378T>G
ENST00000547103.5:c.6059T>G	ENSP00000447211.1:p.Val2020Gly
ENST00000550182.2:c.146T>G	ENSP00000449641.1:p.Val49Gly
ENST00000551340.5:c.250T>G
NM_173591.3:c.6095T>G	NP_775862.3:p.Val2032Gly
XM_005268802.2:c.6146T>G	XP_005268859.1:p.Val2049Gly
XM_011538191.1:c.6146T>G	XP_011536493.1:p.Val2049Gly
XM_011538192.1:c.5993T>G	XP_011536494.1:p.Val1998Gly
XM_011538193.1:c.5780T>G	XP_011536495.1:p.Val1927Gly
XM_005268802.3:c.6146T>G	XP_005268859.1:p.Val2049Gly
XM_011538192.2:c.5993T>G	XP_011536494.1:p.Val1998Gly
NM_001368062.1:c.5960T>G	NP_001354991.1:p.Val1987Gly
NM_001368062.3:c.5987T>G	NP_001354991.2:p.Val1996Gly
NM_001378609.3:c.6122T>G MANE Select	NP_001365538.2:p.Val2041Gly
NM_001378610.3:c.6122T>G	NP_001365539.2:p.Val2041Gly
NM_173591.7:c.6122T>G	NP_775862.4:p.Val2041Gly