Canonical Allele Identifier: CA480823299

Gene: OTOGL

Linked Data

• gnomAD v4: 12-80358726-T-C
• MyVariant Identifiers: chr12:g.80752506T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358726T>C , CM000674.2:g.80358726T>C	GRCh38
NC_000012.11:g.80752506T>C , CM000674.1:g.80752506T>C	GRCh37
NC_000012.10:g.79276637T>C	NCBI36
NG_033008.1:g.154274T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6177T>C MANE Select	ENSP00000447211.2:p.Asn2059=
ENST00000642294.1:c.117T>C	ENSP00000493572.1:p.Asn39=
ENST00000646859.1:c.6042T>C	ENSP00000496036.1:p.Asn2014=
ENST00000298820.7:c.1478T>C
ENST00000458043.6:c.6150T>C	ENSP00000400895.2:p.Asn2050=
ENST00000546620.5:n.433T>C
ENST00000547103.5:c.6114T>C	ENSP00000447211.1:p.Asn2038=
ENST00000550182.2:c.201T>C	ENSP00000449641.1:p.Asn67=
ENST00000551340.5:c.305T>C
NM_173591.3:c.6150T>C	NP_775862.3:p.Asn2050=
XM_005268802.2:c.6201T>C	XP_005268859.1:p.Asn2067=
XM_011538191.1:c.6201T>C	XP_011536493.1:p.Asn2067=
XM_011538192.1:c.6048T>C	XP_011536494.1:p.Asn2016=
XM_011538193.1:c.5835T>C	XP_011536495.1:p.Asn1945=
XM_005268802.3:c.6201T>C	XP_005268859.1:p.Asn2067=
XM_011538192.2:c.6048T>C	XP_011536494.1:p.Asn2016=
NM_001368062.1:c.6015T>C	NP_001354991.1:p.Asn2005=
NM_001368062.3:c.6042T>C	NP_001354991.2:p.Asn2014=
NM_001378609.3:c.6177T>C MANE Select	NP_001365538.2:p.Asn2059=
NM_001378610.3:c.6177T>C	NP_001365539.2:p.Asn2059=
NM_173591.7:c.6177T>C	NP_775862.4:p.Asn2059=