Canonical Allele Identifier: CA480823502

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752542A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358762A>C , CM000674.2:g.80358762A>C	GRCh38
NC_000012.11:g.80752542A>C , CM000674.1:g.80752542A>C	GRCh37
NC_000012.10:g.79276673A>C	NCBI36
NG_033008.1:g.154310A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6213A>C MANE Select	ENSP00000447211.2:p.Pro2071=
ENST00000642294.1:c.153A>C	ENSP00000493572.1:p.Pro51=
ENST00000646859.1:c.6078A>C	ENSP00000496036.1:p.Pro2026=
ENST00000298820.7:c.1514A>C
ENST00000458043.6:c.6186A>C	ENSP00000400895.2:p.Pro2062=
ENST00000546620.5:n.469A>C
ENST00000547103.5:c.6150A>C	ENSP00000447211.1:p.Pro2050=
ENST00000550182.2:c.237A>C	ENSP00000449641.1:p.Pro79=
ENST00000551340.5:c.341A>C
NM_173591.3:c.6186A>C	NP_775862.3:p.Pro2062=
XM_005268802.2:c.6237A>C	XP_005268859.1:p.Pro2079=
XM_011538191.1:c.6237A>C	XP_011536493.1:p.Pro2079=
XM_011538192.1:c.6084A>C	XP_011536494.1:p.Pro2028=
XM_011538193.1:c.5871A>C	XP_011536495.1:p.Pro1957=
XM_005268802.3:c.6237A>C	XP_005268859.1:p.Pro2079=
XM_011538192.2:c.6084A>C	XP_011536494.1:p.Pro2028=
NM_001368062.1:c.6051A>C	NP_001354991.1:p.Pro2017=
NM_001368062.3:c.6078A>C	NP_001354991.2:p.Pro2026=
NM_001378609.3:c.6213A>C MANE Select	NP_001365538.2:p.Pro2071=
NM_001378610.3:c.6213A>C	NP_001365539.2:p.Pro2071=
NM_173591.7:c.6213A>C	NP_775862.4:p.Pro2071=