Canonical Allele Identifier: CA425206626

Gene: OTOF

Linked Data

• gnomAD v4: 2-26482515-T-G
• MyVariant Identifiers: chr2:g.26705383T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482515T>G , CM000664.2:g.26482515T>G	GRCh38
NC_000002.11:g.26705383T>G , CM000664.1:g.26705383T>G	GRCh37
NC_000002.10:g.26558887T>G	NCBI36
NG_009937.1:g.81184A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1470A>C MANE Select	ENSP00000272371.2:p.Pro490=
ENST00000272371.6:c.1470A>C	ENSP00000272371.2:p.Pro490=
ENST00000403946.7:c.1470A>C	ENSP00000385255.3:p.Pro490=
NM_001287489.1:c.1470A>C	NP_001274418.1:p.Pro490=
NM_194248.2:c.1470A>C	NP_919224.1:p.Pro490=
XM_005264644.2:c.1515A>C	XP_005264701.1:p.Pro505=
XM_011533185.1:c.1515A>C	XP_011531487.1:p.Pro505=
XM_017005338.1:c.1470A>C	XP_016860827.1:p.Pro490=
NM_001287489.2:c.1470A>C	NP_001274418.1:p.Pro490=
NM_194248.3:c.1470A>C MANE Select	NP_919224.1:p.Pro490=