Canonical Allele Identifier: CA385888937
Gene: OTOGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80358875A>G , CM000674.2:g.80358875A>G GRCh38
NC_000012.11:g.80752655A>G , CM000674.1:g.80752655A>G GRCh37
NC_000012.10:g.79276786A>G NCBI36
NG_033008.1:g.154423A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000547103.7:c.6242A>G MANE Select ENSP00000447211.2:p.Asn2081Ser
ENST00000642294.1:c.182A>G ENSP00000493572.1:p.Asn61Ser
ENST00000646859.1:c.6107A>G ENSP00000496036.1:p.Asn2036Ser
ENST00000298820.7:c.1527+100A>G
ENST00000458043.6:c.6215A>G ENSP00000400895.2:p.Asn2072Ser
ENST00000546620.5:n.498A>G
ENST00000547103.5:c.6179A>G ENSP00000447211.1:p.Asn2060Ser
ENST00000550182.2:c.266A>G ENSP00000449641.1:p.Asn89Ser
ENST00000551340.5:c.370A>G
NM_173591.3:c.6215A>G NP_775862.3:p.Asn2072Ser
XM_005268802.2:c.6266A>G XP_005268859.1:p.Asn2089Ser
XM_011538191.1:c.6266A>G XP_011536493.1:p.Asn2089Ser
XM_011538192.1:c.6113A>G XP_011536494.1:p.Asn2038Ser
XM_011538193.1:c.5900A>G XP_011536495.1:p.Asn1967Ser
XM_005268802.3:c.6266A>G XP_005268859.1:p.Asn2089Ser
XM_011538192.2:c.6113A>G XP_011536494.1:p.Asn2038Ser
NM_001368062.1:c.6080A>G NP_001354991.1:p.Asn2027Ser
NM_001368062.3:c.6107A>G NP_001354991.2:p.Asn2036Ser
NM_001378609.3:c.6242A>G MANE Select NP_001365538.2:p.Asn2081Ser
NM_001378610.3:c.6242A>G NP_001365539.2:p.Asn2081Ser
NM_173591.7:c.6242A>G NP_775862.4:p.Asn2081Ser