Canonical Allele Identifier: CA480823106

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752470T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358690T>C , CM000674.2:g.80358690T>C	GRCh38
NC_000012.11:g.80752470T>C , CM000674.1:g.80752470T>C	GRCh37
NC_000012.10:g.79276601T>C	NCBI36
NG_033008.1:g.154238T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6141T>C MANE Select	ENSP00000447211.2:p.Cys2047=
ENST00000642294.1:c.81T>C	ENSP00000493572.1:p.Cys27=
ENST00000646859.1:c.6006T>C	ENSP00000496036.1:p.Cys2002=
ENST00000298820.7:c.1442T>C
ENST00000458043.6:c.6114T>C	ENSP00000400895.2:p.Cys2038=
ENST00000546620.5:n.397T>C
ENST00000547103.5:c.6078T>C	ENSP00000447211.1:p.Cys2026=
ENST00000550182.2:c.165T>C	ENSP00000449641.1:p.Cys55=
ENST00000551340.5:c.269T>C
NM_173591.3:c.6114T>C	NP_775862.3:p.Cys2038=
XM_005268802.2:c.6165T>C	XP_005268859.1:p.Cys2055=
XM_011538191.1:c.6165T>C	XP_011536493.1:p.Cys2055=
XM_011538192.1:c.6012T>C	XP_011536494.1:p.Cys2004=
XM_011538193.1:c.5799T>C	XP_011536495.1:p.Cys1933=
XM_005268802.3:c.6165T>C	XP_005268859.1:p.Cys2055=
XM_011538192.2:c.6012T>C	XP_011536494.1:p.Cys2004=
NM_001368062.1:c.5979T>C	NP_001354991.1:p.Cys1993=
NM_001368062.3:c.6006T>C	NP_001354991.2:p.Cys2002=
NM_001378609.3:c.6141T>C MANE Select	NP_001365538.2:p.Cys2047=
NM_001378610.3:c.6141T>C	NP_001365539.2:p.Cys2047=
NM_173591.7:c.6141T>C	NP_775862.4:p.Cys2047=