Canonical Allele Identifier: CA385888874

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752549C>T (hg19) ; chr12:g.80358769C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358769C>T , CM000674.2:g.80358769C>T	GRCh38
NC_000012.11:g.80752549C>T , CM000674.1:g.80752549C>T	GRCh37
NC_000012.10:g.79276680C>T	NCBI36
NG_033008.1:g.154317C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6220C>T MANE Select	ENSP00000447211.2:p.His2074Tyr
ENST00000642294.1:c.160C>T	ENSP00000493572.1:p.His54Tyr
ENST00000646859.1:c.6085C>T	ENSP00000496036.1:p.His2029Tyr
ENST00000298820.7:c.1521C>T
ENST00000458043.6:c.6193C>T	ENSP00000400895.2:p.His2065Tyr
ENST00000546620.5:n.476C>T
ENST00000547103.5:c.6157C>T	ENSP00000447211.1:p.His2053Tyr
ENST00000550182.2:c.244C>T	ENSP00000449641.1:p.His82Tyr
ENST00000551340.5:c.348C>T
NM_173591.3:c.6193C>T	NP_775862.3:p.His2065Tyr
XM_005268802.2:c.6244C>T	XP_005268859.1:p.His2082Tyr
XM_011538191.1:c.6244C>T	XP_011536493.1:p.His2082Tyr
XM_011538192.1:c.6091C>T	XP_011536494.1:p.His2031Tyr
XM_011538193.1:c.5878C>T	XP_011536495.1:p.His1960Tyr
XM_005268802.3:c.6244C>T	XP_005268859.1:p.His2082Tyr
XM_011538192.2:c.6091C>T	XP_011536494.1:p.His2031Tyr
NM_001368062.1:c.6058C>T	NP_001354991.1:p.His2020Tyr
NM_001368062.3:c.6085C>T	NP_001354991.2:p.His2029Tyr
NM_001378609.3:c.6220C>T MANE Select	NP_001365538.2:p.His2074Tyr
NM_001378610.3:c.6220C>T	NP_001365539.2:p.His2074Tyr
NM_173591.7:c.6220C>T	NP_775862.4:p.His2074Tyr