Canonical Allele Identifier: CA346136969
Gene: OTOF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26467184A>G , CM000664.2:g.26467184A>G GRCh38
NC_000002.11:g.26690052A>G , CM000664.1:g.26690052A>G GRCh37
NC_000002.10:g.26543556A>G NCBI36
NG_009937.1:g.96515T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.4277T>C MANE Select ENSP00000272371.2:p.Leu1426Pro
ENST00000339598.8:c.1976T>C MANE Plus Clinical ENSP00000344521.3:p.Leu659Pro
ENST00000402415.8:c.2036T>C ENSP00000383906.4:p.Leu679Pro
ENST00000272371.6:c.4277T>C ENSP00000272371.2:p.Leu1426Pro
ENST00000338581.10:c.1976T>C ENSP00000345137.6:p.Leu659Pro
ENST00000339598.7:c.1976T>C ENSP00000344521.3:p.Leu659Pro
ENST00000402415.7:c.2207T>C ENSP00000383906.3:p.Leu736Pro
ENST00000403946.7:c.4277T>C ENSP00000385255.3:p.Leu1426Pro
NM_001287489.1:c.4277T>C NP_001274418.1:p.Leu1426Pro
NM_004802.3:c.1976T>C NP_004793.2:p.Leu659Pro
NM_194248.2:c.4277T>C NP_919224.1:p.Leu1426Pro
NM_194322.2:c.2207T>C NP_919303.1:p.Leu736Pro
NM_194323.2:c.1976T>C NP_919304.1:p.Leu659Pro
XM_005264644.2:c.4262T>C XP_005264701.1:p.Leu1421Pro
XM_011533185.1:c.4322T>C XP_011531487.1:p.Leu1441Pro
XM_017005338.1:c.4217T>C XP_016860827.1:p.Leu1406Pro
NM_001287489.2:c.4277T>C NP_001274418.1:p.Leu1426Pro
NM_004802.4:c.1976T>C NP_004793.2:p.Leu659Pro
NM_194248.3:c.4277T>C MANE Select NP_919224.1:p.Leu1426Pro
NM_194322.3:c.2207T>C NP_919303.1:p.Leu736Pro
NM_194323.3:c.1976T>C MANE Plus Clinical NP_919304.1:p.Leu659Pro