Canonical Allele Identifier: CA346137259

Gene: OTOF

Linked Data

• dbSNP Id: rs1212517593
• gnomAD v2: 2-26690271-C-A
• gnomAD v4: 2-26467403-C-A
• MyVariant Identifiers: chr2:g.26690271C>A (hg19) ; chr2:g.26467403C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467403C>A , CM000664.2:g.26467403C>A	GRCh38
NC_000002.11:g.26690271C>A , CM000664.1:g.26690271C>A	GRCh37
NC_000002.10:g.26543775C>A	NCBI36
NG_009937.1:g.96296G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4189G>T MANE Select	ENSP00000272371.2:p.Ala1397Ser
ENST00000339598.8:c.1888G>T MANE Plus Clinical	ENSP00000344521.3:p.Ala630Ser
ENST00000402415.8:c.1948G>T	ENSP00000383906.4:p.Ala650Ser
ENST00000272371.6:c.4189G>T	ENSP00000272371.2:p.Ala1397Ser
ENST00000338581.10:c.1888G>T	ENSP00000345137.6:p.Ala630Ser
ENST00000339598.7:c.1888G>T	ENSP00000344521.3:p.Ala630Ser
ENST00000402415.7:c.2119G>T	ENSP00000383906.3:p.Ala707Ser
ENST00000403946.7:c.4189G>T	ENSP00000385255.3:p.Ala1397Ser
NM_001287489.1:c.4189G>T	NP_001274418.1:p.Ala1397Ser
NM_004802.3:c.1888G>T	NP_004793.2:p.Ala630Ser
NM_194248.2:c.4189G>T	NP_919224.1:p.Ala1397Ser
NM_194322.2:c.2119G>T	NP_919303.1:p.Ala707Ser
NM_194323.2:c.1888G>T	NP_919304.1:p.Ala630Ser
XM_005264644.2:c.4174G>T	XP_005264701.1:p.Ala1392Ser
XM_011533185.1:c.4234G>T	XP_011531487.1:p.Ala1412Ser
XM_017005338.1:c.4129G>T	XP_016860827.1:p.Ala1377Ser
NM_001287489.2:c.4189G>T	NP_001274418.1:p.Ala1397Ser
NM_004802.4:c.1888G>T	NP_004793.2:p.Ala630Ser
NM_194248.3:c.4189G>T MANE Select	NP_919224.1:p.Ala1397Ser
NM_194322.3:c.2119G>T	NP_919303.1:p.Ala707Ser
NM_194323.3:c.1888G>T MANE Plus Clinical	NP_919304.1:p.Ala630Ser