Canonical Allele Identifier: CA385888745

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752492G>T (hg19) ; chr12:g.80358712G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358712G>T , CM000674.2:g.80358712G>T	GRCh38
NC_000012.11:g.80752492G>T , CM000674.1:g.80752492G>T	GRCh37
NC_000012.10:g.79276623G>T	NCBI36
NG_033008.1:g.154260G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6163G>T MANE Select	ENSP00000447211.2:p.Ala2055Ser
ENST00000642294.1:c.103G>T	ENSP00000493572.1:p.Ala35Ser
ENST00000646859.1:c.6028G>T	ENSP00000496036.1:p.Ala2010Ser
ENST00000298820.7:c.1464G>T
ENST00000458043.6:c.6136G>T	ENSP00000400895.2:p.Ala2046Ser
ENST00000546620.5:n.419G>T
ENST00000547103.5:c.6100G>T	ENSP00000447211.1:p.Ala2034Ser
ENST00000550182.2:c.187G>T	ENSP00000449641.1:p.Ala63Ser
ENST00000551340.5:c.291G>T
NM_173591.3:c.6136G>T	NP_775862.3:p.Ala2046Ser
XM_005268802.2:c.6187G>T	XP_005268859.1:p.Ala2063Ser
XM_011538191.1:c.6187G>T	XP_011536493.1:p.Ala2063Ser
XM_011538192.1:c.6034G>T	XP_011536494.1:p.Ala2012Ser
XM_011538193.1:c.5821G>T	XP_011536495.1:p.Ala1941Ser
XM_005268802.3:c.6187G>T	XP_005268859.1:p.Ala2063Ser
XM_011538192.2:c.6034G>T	XP_011536494.1:p.Ala2012Ser
NM_001368062.1:c.6001G>T	NP_001354991.1:p.Ala2001Ser
NM_001368062.3:c.6028G>T	NP_001354991.2:p.Ala2010Ser
NM_001378609.3:c.6163G>T MANE Select	NP_001365538.2:p.Ala2055Ser
NM_001378610.3:c.6163G>T	NP_001365539.2:p.Ala2055Ser
NM_173591.7:c.6163G>T	NP_775862.4:p.Ala2055Ser