Canonical Allele Identifier: CA480823202

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752488C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358708C>T , CM000674.2:g.80358708C>T	GRCh38
NC_000012.11:g.80752488C>T , CM000674.1:g.80752488C>T	GRCh37
NC_000012.10:g.79276619C>T	NCBI36
NG_033008.1:g.154256C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6159C>T MANE Select	ENSP00000447211.2:p.Asn2053=
ENST00000642294.1:c.99C>T	ENSP00000493572.1:p.Asn33=
ENST00000646859.1:c.6024C>T	ENSP00000496036.1:p.Asn2008=
ENST00000298820.7:c.1460C>T
ENST00000458043.6:c.6132C>T	ENSP00000400895.2:p.Asn2044=
ENST00000546620.5:n.415C>T
ENST00000547103.5:c.6096C>T	ENSP00000447211.1:p.Asn2032=
ENST00000550182.2:c.183C>T	ENSP00000449641.1:p.Asn61=
ENST00000551340.5:c.287C>T
NM_173591.3:c.6132C>T	NP_775862.3:p.Asn2044=
XM_005268802.2:c.6183C>T	XP_005268859.1:p.Asn2061=
XM_011538191.1:c.6183C>T	XP_011536493.1:p.Asn2061=
XM_011538192.1:c.6030C>T	XP_011536494.1:p.Asn2010=
XM_011538193.1:c.5817C>T	XP_011536495.1:p.Asn1939=
XM_005268802.3:c.6183C>T	XP_005268859.1:p.Asn2061=
XM_011538192.2:c.6030C>T	XP_011536494.1:p.Asn2010=
NM_001368062.1:c.5997C>T	NP_001354991.1:p.Asn1999=
NM_001368062.3:c.6024C>T	NP_001354991.2:p.Asn2008=
NM_001378609.3:c.6159C>T MANE Select	NP_001365538.2:p.Asn2053=
NM_001378610.3:c.6159C>T	NP_001365539.2:p.Asn2053=
NM_173591.7:c.6159C>T	NP_775862.4:p.Asn2053=