Canonical Allele Identifier: CA346137842

Gene: OTOF

Linked Data

• gnomAD v4: 2-26484561-A-G
• MyVariant Identifiers: chr2:g.26707429A>G (hg19) ; chr2:g.26484561A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26484561A>G , CM000664.2:g.26484561A>G	GRCh38
NC_000002.11:g.26707429A>G , CM000664.1:g.26707429A>G	GRCh37
NC_000002.10:g.26560933A>G	NCBI36
NG_009937.1:g.79138T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1118T>C MANE Select	ENSP00000272371.2:p.Val373Ala
ENST00000272371.6:c.1118T>C	ENSP00000272371.2:p.Val373Ala
ENST00000403946.7:c.1118T>C	ENSP00000385255.3:p.Val373Ala
NM_001287489.1:c.1118T>C	NP_001274418.1:p.Val373Ala
NM_194248.2:c.1118T>C	NP_919224.1:p.Val373Ala
XM_005264644.2:c.1163T>C	XP_005264701.1:p.Val388Ala
XM_011533185.1:c.1163T>C	XP_011531487.1:p.Val388Ala
XM_017005338.1:c.1118T>C	XP_016860827.1:p.Val373Ala
NM_001287489.2:c.1118T>C	NP_001274418.1:p.Val373Ala
NM_194248.3:c.1118T>C MANE Select	NP_919224.1:p.Val373Ala