Canonical Allele Identifier: CA385850041

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80632658T>C (hg19) ; chr12:g.80238878T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80238878T>C , CM000674.2:g.80238878T>C	GRCh38
NC_000012.11:g.80632658T>C , CM000674.1:g.80632658T>C	GRCh37
NC_000012.10:g.79156789T>C	NCBI36
NG_033008.1:g.34426T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000547103.7:c.845T>C MANE Select	ENSP00000447211.2:p.Phe282Ser
ENST00000643417.1:n.1505T>C
ENST00000646859.1:c.845T>C	ENSP00000496036.1:p.Phe282Ser
ENST00000458043.6:c.818T>C	ENSP00000400895.2:p.Phe273Ser
ENST00000547103.5:c.818T>C	ENSP00000447211.1:p.Phe273Ser
NM_173591.3:c.818T>C	NP_775862.3:p.Phe273Ser
XM_005268802.2:c.869T>C	XP_005268859.1:p.Phe290Ser
XM_011538191.1:c.869T>C	XP_011536493.1:p.Phe290Ser
XM_011538192.1:c.716T>C	XP_011536494.1:p.Phe239Ser
XM_011538193.1:c.503T>C	XP_011536495.1:p.Phe168Ser
XM_005268802.3:c.869T>C	XP_005268859.1:p.Phe290Ser
XM_011538192.2:c.716T>C	XP_011536494.1:p.Phe239Ser
NM_001368062.1:c.818T>C	NP_001354991.1:p.Phe273Ser
NM_001368062.3:c.845T>C	NP_001354991.2:p.Phe282Ser
NM_001378609.3:c.845T>C MANE Select	NP_001365538.2:p.Phe282Ser
NM_001378610.3:c.845T>C	NP_001365539.2:p.Phe282Ser
NM_173591.7:c.845T>C	NP_775862.4:p.Phe282Ser