Canonical Allele Identifier: CA346135217

Gene: OTOF

Linked Data

• gnomAD v4: 2-26465676-A-C
• MyVariant Identifiers: chr2:g.26688544A>C (hg19) ; chr2:g.26465676A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26465676A>C , CM000664.2:g.26465676A>C	GRCh38
NC_000002.11:g.26688544A>C , CM000664.1:g.26688544A>C	GRCh37
NC_000002.10:g.26542048A>C	NCBI36
NG_009937.1:g.98023T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.4795T>G MANE Select	ENSP00000272371.2:p.Ser1599Ala
ENST00000339598.8:c.2494T>G MANE Plus Clinical	ENSP00000344521.3:p.Ser832Ala
ENST00000402415.8:c.2554T>G	ENSP00000383906.4:p.Ser852Ala
ENST00000272371.6:c.4795T>G	ENSP00000272371.2:p.Ser1599Ala
ENST00000338581.10:c.2494T>G	ENSP00000345137.6:p.Ser832Ala
ENST00000339598.7:c.2494T>G	ENSP00000344521.3:p.Ser832Ala
ENST00000402415.7:c.2725T>G	ENSP00000383906.3:p.Ser909Ala
ENST00000403946.7:c.4795T>G	ENSP00000385255.3:p.Ser1599Ala
ENST00000464574.1:n.544T>G
NM_001287489.1:c.4795T>G	NP_001274418.1:p.Ser1599Ala
NM_004802.3:c.2494T>G	NP_004793.2:p.Ser832Ala
NM_194248.2:c.4795T>G	NP_919224.1:p.Ser1599Ala
NM_194322.2:c.2725T>G	NP_919303.1:p.Ser909Ala
NM_194323.2:c.2494T>G	NP_919304.1:p.Ser832Ala
XM_005264644.2:c.4780T>G	XP_005264701.1:p.Ser1594Ala
XM_011533185.1:c.4840T>G	XP_011531487.1:p.Ser1614Ala
XM_017005338.1:c.4735T>G	XP_016860827.1:p.Ser1579Ala
NM_001287489.2:c.4795T>G	NP_001274418.1:p.Ser1599Ala
NM_004802.4:c.2494T>G	NP_004793.2:p.Ser832Ala
NM_194248.3:c.4795T>G MANE Select	NP_919224.1:p.Ser1599Ala
NM_194322.3:c.2725T>G	NP_919303.1:p.Ser909Ala
NM_194323.3:c.2494T>G MANE Plus Clinical	NP_919304.1:p.Ser832Ala