Canonical Allele Identifier: CA385888957

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752664T>G (hg19) ; chr12:g.80358884T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358884T>G , CM000674.2:g.80358884T>G	GRCh38
NC_000012.11:g.80752664T>G , CM000674.1:g.80752664T>G	GRCh37
NC_000012.10:g.79276795T>G	NCBI36
NG_033008.1:g.154432T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6251T>G MANE Select	ENSP00000447211.2:p.Met2084Arg
ENST00000642294.1:c.191T>G	ENSP00000493572.1:p.Met64Arg
ENST00000646859.1:c.6116T>G	ENSP00000496036.1:p.Met2039Arg
ENST00000298820.7:c.1527+109T>G
ENST00000458043.6:c.6224T>G	ENSP00000400895.2:p.Met2075Arg
ENST00000546620.5:n.507T>G
ENST00000547103.5:c.6188T>G	ENSP00000447211.1:p.Met2063Arg
ENST00000550182.2:c.275T>G	ENSP00000449641.1:p.Met92Arg
ENST00000551340.5:c.379T>G
NM_173591.3:c.6224T>G	NP_775862.3:p.Met2075Arg
XM_005268802.2:c.6275T>G	XP_005268859.1:p.Met2092Arg
XM_011538191.1:c.6275T>G	XP_011536493.1:p.Met2092Arg
XM_011538192.1:c.6122T>G	XP_011536494.1:p.Met2041Arg
XM_011538193.1:c.5909T>G	XP_011536495.1:p.Met1970Arg
XM_005268802.3:c.6275T>G	XP_005268859.1:p.Met2092Arg
XM_011538192.2:c.6122T>G	XP_011536494.1:p.Met2041Arg
NM_001368062.1:c.6089T>G	NP_001354991.1:p.Met2030Arg
NM_001368062.3:c.6116T>G	NP_001354991.2:p.Met2039Arg
NM_001378609.3:c.6251T>G MANE Select	NP_001365538.2:p.Met2084Arg
NM_001378610.3:c.6251T>G	NP_001365539.2:p.Met2084Arg
NM_173591.7:c.6251T>G	NP_775862.4:p.Met2084Arg