Canonical Allele Identifier: CA531396563

Gene: OTOF

Linked Data

• dbSNP Id: rs1431126460
• gnomAD v2: 2-26706628-A-G
• gnomAD v3: 2-26483760-A-G
• gnomAD v4: 2-26483760-A-G
• MyVariant Identifiers: chr2:g.26706628A>G (hg19) ; chr2:g.26483760A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26483760A>G , CM000664.2:g.26483760A>G	GRCh38
NC_000002.11:g.26706628A>G , CM000664.1:g.26706628A>G	GRCh37
NC_000002.10:g.26560132A>G	NCBI36
NG_009937.1:g.79939T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1206-112T>C MANE Select	ENSP00000272371.2:n.1206-112T>C
ENST00000272371.6:c.1206-112T>C	ENSP00000272371.2:n.1206-112T>C
ENST00000403946.7:c.1206-112T>C	ENSP00000385255.3:n.1206-112T>C
NM_001287489.1:c.1206-112T>C	NP_001274418.1:n.1206-112T>C
NM_194248.2:c.1206-112T>C	NP_919224.1:n.1206-112T>C
XM_005264644.2:c.1251-112T>C	XP_005264701.1:n.1251-112T>C
XM_011533185.1:c.1251-112T>C	XP_011531487.1:n.1251-112T>C
XM_017005338.1:c.1206-112T>C	XP_016860827.1:n.1206-112T>C
NM_001287489.2:c.1206-112T>C	NP_001274418.1:n.1206-112T>C
NM_194248.3:c.1206-112T>C MANE Select	NP_919224.1:n.1206-112T>C