Canonical Allele Identifier: CA385888963

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752667C>G (hg19) ; chr12:g.80358887C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358887C>G , CM000674.2:g.80358887C>G	GRCh38
NC_000012.11:g.80752667C>G , CM000674.1:g.80752667C>G	GRCh37
NC_000012.10:g.79276798C>G	NCBI36
NG_033008.1:g.154435C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6254C>G MANE Select	ENSP00000447211.2:p.Pro2085Arg
ENST00000642294.1:c.194C>G	ENSP00000493572.1:p.Pro65Arg
ENST00000646859.1:c.6119C>G	ENSP00000496036.1:p.Pro2040Arg
ENST00000298820.7:c.1527+112C>G
ENST00000458043.6:c.6227C>G	ENSP00000400895.2:p.Pro2076Arg
ENST00000546620.5:n.510C>G
ENST00000547103.5:c.6191C>G	ENSP00000447211.1:p.Pro2064Arg
ENST00000550182.2:c.278C>G	ENSP00000449641.1:p.Pro93Arg
ENST00000551340.5:c.382C>G
NM_173591.3:c.6227C>G	NP_775862.3:p.Pro2076Arg
XM_005268802.2:c.6278C>G	XP_005268859.1:p.Pro2093Arg
XM_011538191.1:c.6278C>G	XP_011536493.1:p.Pro2093Arg
XM_011538192.1:c.6125C>G	XP_011536494.1:p.Pro2042Arg
XM_011538193.1:c.5912C>G	XP_011536495.1:p.Pro1971Arg
XM_005268802.3:c.6278C>G	XP_005268859.1:p.Pro2093Arg
XM_011538192.2:c.6125C>G	XP_011536494.1:p.Pro2042Arg
NM_001368062.1:c.6092C>G	NP_001354991.1:p.Pro2031Arg
NM_001368062.3:c.6119C>G	NP_001354991.2:p.Pro2040Arg
NM_001378609.3:c.6254C>G MANE Select	NP_001365538.2:p.Pro2085Arg
NM_001378610.3:c.6254C>G	NP_001365539.2:p.Pro2085Arg
NM_173591.7:c.6254C>G	NP_775862.4:p.Pro2085Arg