Canonical Allele Identifier: CA425205993
Gene: OTOF HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.26703750G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26480882G>A , CM000664.2:g.26480882G>A GRCh38
NC_000002.11:g.26703750G>A , CM000664.1:g.26703750G>A GRCh37
NC_000002.10:g.26557254G>A NCBI36
NG_009937.1:g.82817C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.1707C>T MANE Select ENSP00000272371.2:p.Leu569=
ENST00000272371.6:c.1707C>T ENSP00000272371.2:p.Leu569=
ENST00000403946.7:c.1707C>T ENSP00000385255.3:p.Leu569=
NM_001287489.1:c.1707C>T NP_001274418.1:p.Leu569=
NM_194248.2:c.1707C>T NP_919224.1:p.Leu569=
XM_005264644.2:c.1752C>T XP_005264701.1:p.Leu584=
XM_011533185.1:c.1752C>T XP_011531487.1:p.Leu584=
XM_017005338.1:c.1707C>T XP_016860827.1:p.Leu569=
NM_001287489.2:c.1707C>T NP_001274418.1:p.Leu569=
NM_194248.3:c.1707C>T MANE Select NP_919224.1:p.Leu569=