Canonical Allele Identifier: CA767291181

Gene: OTOF

Linked Data

• dbSNP Id: rs1453256011
• MyVariant Identifiers: chr2:g.26706658_26706670del (hg19) ; chr2:g.26483790_26483802del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26483790_26483802del , CM000664.2:g.26483790_26483802del	GRCh38
NC_000002.11:g.26706658_26706670del , CM000664.1:g.26706658_26706670del	GRCh37
NC_000002.10:g.26560162_26560174del	NCBI36
NG_009937.1:g.79897_79909del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1206-154_1206-142del MANE Select	ENSP00000272371.2:n.1206-154_1206-142del
ENST00000272371.6:c.1206-154_1206-142del	ENSP00000272371.2:n.1206-154_1206-142del
ENST00000403946.7:c.1206-154_1206-142del	ENSP00000385255.3:n.1206-154_1206-142del
NM_001287489.1:c.1206-154_1206-142del	NP_001274418.1:n.1206-154_1206-142del
NM_194248.2:c.1206-154_1206-142del	NP_919224.1:n.1206-154_1206-142del
XM_005264644.2:c.1251-154_1251-142del	XP_005264701.1:n.1251-154_1251-142del
XM_011533185.1:c.1251-154_1251-142del	XP_011531487.1:n.1251-154_1251-142del
XM_017005338.1:c.1206-154_1206-142del	XP_016860827.1:n.1206-154_1206-142del
NM_001287489.2:c.1206-154_1206-142del	NP_001274418.1:n.1206-154_1206-142del
NM_194248.3:c.1206-154_1206-142del MANE Select	NP_919224.1:n.1206-154_1206-142del