Canonical Allele Identifier: CA385888628

Gene: OTOGL

Linked Data

• gnomAD v4: 12-80358346-T-C
• MyVariant Identifiers: chr12:g.80752126T>C (hg19) ; chr12:g.80358346T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358346T>C , CM000674.2:g.80358346T>C	GRCh38
NC_000012.11:g.80752126T>C , CM000674.1:g.80752126T>C	GRCh37
NC_000012.10:g.79276257T>C	NCBI36
NG_033008.1:g.153894T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6118T>C MANE Select	ENSP00000447211.2:p.Cys2040Arg
ENST00000642294.1:c.58T>C	ENSP00000493572.1:p.Cys20Arg
ENST00000646859.1:c.5983T>C	ENSP00000496036.1:p.Cys1995Arg
ENST00000298820.7:c.1419T>C
ENST00000458043.6:c.6091T>C	ENSP00000400895.2:p.Cys2031Arg
ENST00000546620.5:n.374T>C
ENST00000547103.5:c.6055T>C	ENSP00000447211.1:p.Cys2019Arg
ENST00000550182.2:c.142T>C	ENSP00000449641.1:p.Cys48Arg
ENST00000551340.5:c.246T>C
NM_173591.3:c.6091T>C	NP_775862.3:p.Cys2031Arg
XM_005268802.2:c.6142T>C	XP_005268859.1:p.Cys2048Arg
XM_011538191.1:c.6142T>C	XP_011536493.1:p.Cys2048Arg
XM_011538192.1:c.5989T>C	XP_011536494.1:p.Cys1997Arg
XM_011538193.1:c.5776T>C	XP_011536495.1:p.Cys1926Arg
XM_005268802.3:c.6142T>C	XP_005268859.1:p.Cys2048Arg
XM_011538192.2:c.5989T>C	XP_011536494.1:p.Cys1997Arg
NM_001368062.1:c.5956T>C	NP_001354991.1:p.Cys1986Arg
NM_001368062.3:c.5983T>C	NP_001354991.2:p.Cys1995Arg
NM_001378609.3:c.6118T>C MANE Select	NP_001365538.2:p.Cys2040Arg
NM_001378610.3:c.6118T>C	NP_001365539.2:p.Cys2040Arg
NM_173591.7:c.6118T>C	NP_775862.4:p.Cys2040Arg