Canonical Allele Identifier: CA6702064
Community Standard Title: NM_001378609.3(OTOGL):c.6511-17A>G
Gene: OTOGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80368188A>G , CM000674.2:g.80368188A>G GRCh38
NC_000012.11:g.80761968A>G , CM000674.1:g.80761968A>G GRCh37
NC_000012.10:g.79286099A>G NCBI36
NG_033008.1:g.163736A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001378609.3:c.6511-17A>G MANE Select NP_001365538.2:n.6511-17A>G
ENST00000547103.7:c.6511-17A>G MANE Select ENSP00000447211.2:n.6511-17A>G
NM_001368062.1:c.6349-17A>G NP_001354991.1:n.6349-17A>G
NM_001368062.3:c.6376-17A>G NP_001354991.2:n.6376-17A>G
NM_001378610.3:c.6511-17A>G NP_001365539.2:n.6511-17A>G
NM_173591.3:c.6484-17A>G NP_775862.3:n.6484-17A>G
NM_173591.7:c.6511-17A>G NP_775862.4:n.6511-17A>G
ENST00000298820.7:c.1707-17A>G
ENST00000458043.6:c.6484-17A>G ENSP00000400895.2:n.6484-17A>G
ENST00000546620.5:n.767-17A>G
ENST00000547103.5:c.6448-17A>G ENSP00000447211.1:n.6448-17A>G
ENST00000550182.2:c.535-17A>G ENSP00000449641.1:n.535-17A>G
ENST00000550182.3:c.40-17A>G ENSP00000449641.2:n.40-17A>G
ENST00000551340.5:c.725-17A>G
ENST00000642294.1:c.569-17A>G ENSP00000493572.1:n.569-17A>G
ENST00000646859.1:c.6376-17A>G ENSP00000496036.1:n.6376-17A>G
XM_005268802.2:c.6535-17A>G XP_005268859.1:n.6535-17A>G
XM_005268802.3:c.6535-17A>G XP_005268859.1:n.6535-17A>G
XM_011538191.1:c.6535-17A>G XP_011536493.1:n.6535-17A>G
XM_011538192.1:c.6382-17A>G XP_011536494.1:n.6382-17A>G
XM_011538192.2:c.6382-17A>G XP_011536494.1:n.6382-17A>G
XM_011538193.1:c.6169-17A>G XP_011536495.1:n.6169-17A>G