Canonical Allele Identifier: CA385888671

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752460C>G (hg19) ; chr12:g.80358680C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358680C>G , CM000674.2:g.80358680C>G	GRCh38
NC_000012.11:g.80752460C>G , CM000674.1:g.80752460C>G	GRCh37
NC_000012.10:g.79276591C>G	NCBI36
NG_033008.1:g.154228C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6131C>G MANE Select	ENSP00000447211.2:p.Pro2044Arg
ENST00000642294.1:c.71C>G	ENSP00000493572.1:p.Pro24Arg
ENST00000646859.1:c.5996C>G	ENSP00000496036.1:p.Pro1999Arg
ENST00000298820.7:c.1432C>G
ENST00000458043.6:c.6104C>G	ENSP00000400895.2:p.Pro2035Arg
ENST00000546620.5:n.387C>G
ENST00000547103.5:c.6068C>G	ENSP00000447211.1:p.Pro2023Arg
ENST00000550182.2:c.155C>G	ENSP00000449641.1:p.Pro52Arg
ENST00000551340.5:c.259C>G
NM_173591.3:c.6104C>G	NP_775862.3:p.Pro2035Arg
XM_005268802.2:c.6155C>G	XP_005268859.1:p.Pro2052Arg
XM_011538191.1:c.6155C>G	XP_011536493.1:p.Pro2052Arg
XM_011538192.1:c.6002C>G	XP_011536494.1:p.Pro2001Arg
XM_011538193.1:c.5789C>G	XP_011536495.1:p.Pro1930Arg
XM_005268802.3:c.6155C>G	XP_005268859.1:p.Pro2052Arg
XM_011538192.2:c.6002C>G	XP_011536494.1:p.Pro2001Arg
NM_001368062.1:c.5969C>G	NP_001354991.1:p.Pro1990Arg
NM_001368062.3:c.5996C>G	NP_001354991.2:p.Pro1999Arg
NM_001378609.3:c.6131C>G MANE Select	NP_001365538.2:p.Pro2044Arg
NM_001378610.3:c.6131C>G	NP_001365539.2:p.Pro2044Arg
NM_173591.7:c.6131C>G	NP_775862.4:p.Pro2044Arg