Canonical Allele Identifier: CA385888895

Gene: OTOGL

Linked Data

• MyVariant Identifiers: chr12:g.80752638A>C (hg19) ; chr12:g.80358858A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358858A>C , CM000674.2:g.80358858A>C	GRCh38
NC_000012.11:g.80752638A>C , CM000674.1:g.80752638A>C	GRCh37
NC_000012.10:g.79276769A>C	NCBI36
NG_033008.1:g.154406A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6227-2A>C MANE Select	ENSP00000447211.2:n.6227-2A>C
ENST00000642294.1:c.167-2A>C	ENSP00000493572.1:n.167-2A>C
ENST00000646859.1:c.6092-2A>C	ENSP00000496036.1:n.6092-2A>C
ENST00000298820.7:c.1527+83A>C
ENST00000458043.6:c.6200-2A>C	ENSP00000400895.2:n.6200-2A>C
ENST00000546620.5:n.483-2A>C
ENST00000547103.5:c.6164-2A>C	ENSP00000447211.1:n.6164-2A>C
ENST00000550182.2:c.251-2A>C	ENSP00000449641.1:n.251-2A>C
ENST00000551340.5:c.355-2A>C
NM_173591.3:c.6200-2A>C	NP_775862.3:n.6200-2A>C
XM_005268802.2:c.6251-2A>C	XP_005268859.1:n.6251-2A>C
XM_011538191.1:c.6251-2A>C	XP_011536493.1:n.6251-2A>C
XM_011538192.1:c.6098-2A>C	XP_011536494.1:n.6098-2A>C
XM_011538193.1:c.5885-2A>C	XP_011536495.1:n.5885-2A>C
XM_005268802.3:c.6251-2A>C	XP_005268859.1:n.6251-2A>C
XM_011538192.2:c.6098-2A>C	XP_011536494.1:n.6098-2A>C
NM_001368062.1:c.6065-2A>C	NP_001354991.1:n.6065-2A>C
NM_001368062.3:c.6092-2A>C	NP_001354991.2:n.6092-2A>C
NM_001378609.3:c.6227-2A>C MANE Select	NP_001365538.2:n.6227-2A>C
NM_001378610.3:c.6227-2A>C	NP_001365539.2:n.6227-2A>C
NM_173591.7:c.6227-2A>C	NP_775862.4:n.6227-2A>C