Canonical Allele Identifier: CA385888722

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752483C>A (hg19) ; chr12:g.80358703C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358703C>A , CM000674.2:g.80358703C>A	GRCh38
NC_000012.11:g.80752483C>A , CM000674.1:g.80752483C>A	GRCh37
NC_000012.10:g.79276614C>A	NCBI36
NG_033008.1:g.154251C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6154C>A MANE Select	ENSP00000447211.2:p.Leu2052Ile
ENST00000642294.1:c.94C>A	ENSP00000493572.1:p.Leu32Ile
ENST00000646859.1:c.6019C>A	ENSP00000496036.1:p.Leu2007Ile
ENST00000298820.7:c.1455C>A
ENST00000458043.6:c.6127C>A	ENSP00000400895.2:p.Leu2043Ile
ENST00000546620.5:n.410C>A
ENST00000547103.5:c.6091C>A	ENSP00000447211.1:p.Leu2031Ile
ENST00000550182.2:c.178C>A	ENSP00000449641.1:p.Leu60Ile
ENST00000551340.5:c.282C>A
NM_173591.3:c.6127C>A	NP_775862.3:p.Leu2043Ile
XM_005268802.2:c.6178C>A	XP_005268859.1:p.Leu2060Ile
XM_011538191.1:c.6178C>A	XP_011536493.1:p.Leu2060Ile
XM_011538192.1:c.6025C>A	XP_011536494.1:p.Leu2009Ile
XM_011538193.1:c.5812C>A	XP_011536495.1:p.Leu1938Ile
XM_005268802.3:c.6178C>A	XP_005268859.1:p.Leu2060Ile
XM_011538192.2:c.6025C>A	XP_011536494.1:p.Leu2009Ile
NM_001368062.1:c.5992C>A	NP_001354991.1:p.Leu1998Ile
NM_001368062.3:c.6019C>A	NP_001354991.2:p.Leu2007Ile
NM_001378609.3:c.6154C>A MANE Select	NP_001365538.2:p.Leu2052Ile
NM_001378610.3:c.6154C>A	NP_001365539.2:p.Leu2052Ile
NM_173591.7:c.6154C>A	NP_775862.4:p.Leu2052Ile