Canonical Allele Identifier: CA385888674

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752462A>G (hg19) ; chr12:g.80358682A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358682A>G , CM000674.2:g.80358682A>G	GRCh38
NC_000012.11:g.80752462A>G , CM000674.1:g.80752462A>G	GRCh37
NC_000012.10:g.79276593A>G	NCBI36
NG_033008.1:g.154230A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6133A>G MANE Select	ENSP00000447211.2:p.Asn2045Asp
ENST00000642294.1:c.73A>G	ENSP00000493572.1:p.Asn25Asp
ENST00000646859.1:c.5998A>G	ENSP00000496036.1:p.Asn2000Asp
ENST00000298820.7:c.1434A>G
ENST00000458043.6:c.6106A>G	ENSP00000400895.2:p.Asn2036Asp
ENST00000546620.5:n.389A>G
ENST00000547103.5:c.6070A>G	ENSP00000447211.1:p.Asn2024Asp
ENST00000550182.2:c.157A>G	ENSP00000449641.1:p.Asn53Asp
ENST00000551340.5:c.261A>G
NM_173591.3:c.6106A>G	NP_775862.3:p.Asn2036Asp
XM_005268802.2:c.6157A>G	XP_005268859.1:p.Asn2053Asp
XM_011538191.1:c.6157A>G	XP_011536493.1:p.Asn2053Asp
XM_011538192.1:c.6004A>G	XP_011536494.1:p.Asn2002Asp
XM_011538193.1:c.5791A>G	XP_011536495.1:p.Asn1931Asp
XM_005268802.3:c.6157A>G	XP_005268859.1:p.Asn2053Asp
XM_011538192.2:c.6004A>G	XP_011536494.1:p.Asn2002Asp
NM_001368062.1:c.5971A>G	NP_001354991.1:p.Asn1991Asp
NM_001368062.3:c.5998A>G	NP_001354991.2:p.Asn2000Asp
NM_001378609.3:c.6133A>G MANE Select	NP_001365538.2:p.Asn2045Asp
NM_001378610.3:c.6133A>G	NP_001365539.2:p.Asn2045Asp
NM_173591.7:c.6133A>G	NP_775862.4:p.Asn2045Asp