Canonical Allele Identifier: CA425359376

Gene: OTOF

Linked Data

• MyVariant Identifiers: chr2:g.26688548G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26465680G>A , CM000664.2:g.26465680G>A	GRCh38
NC_000002.11:g.26688548G>A , CM000664.1:g.26688548G>A	GRCh37
NC_000002.10:g.26542052G>A	NCBI36
NG_009937.1:g.98019C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4791C>T MANE Select	ENSP00000272371.2:p.Thr1597=
ENST00000339598.8:c.2490C>T MANE Plus Clinical	ENSP00000344521.3:p.Thr830=
ENST00000402415.8:c.2550C>T	ENSP00000383906.4:p.Thr850=
ENST00000272371.6:c.4791C>T	ENSP00000272371.2:p.Thr1597=
ENST00000338581.10:c.2490C>T	ENSP00000345137.6:p.Thr830=
ENST00000339598.7:c.2490C>T	ENSP00000344521.3:p.Thr830=
ENST00000402415.7:c.2721C>T	ENSP00000383906.3:p.Thr907=
ENST00000403946.7:c.4791C>T	ENSP00000385255.3:p.Thr1597=
ENST00000464574.1:n.540C>T
NM_001287489.1:c.4791C>T	NP_001274418.1:p.Thr1597=
NM_004802.3:c.2490C>T	NP_004793.2:p.Thr830=
NM_194248.2:c.4791C>T	NP_919224.1:p.Thr1597=
NM_194322.2:c.2721C>T	NP_919303.1:p.Thr907=
NM_194323.2:c.2490C>T	NP_919304.1:p.Thr830=
XM_005264644.2:c.4776C>T	XP_005264701.1:p.Thr1592=
XM_011533185.1:c.4836C>T	XP_011531487.1:p.Thr1612=
XM_017005338.1:c.4731C>T	XP_016860827.1:p.Thr1577=
NM_001287489.2:c.4791C>T	NP_001274418.1:p.Thr1597=
NM_004802.4:c.2490C>T	NP_004793.2:p.Thr830=
NM_194248.3:c.4791C>T MANE Select	NP_919224.1:p.Thr1597=
NM_194322.3:c.2721C>T	NP_919303.1:p.Thr907=
NM_194323.3:c.2490C>T MANE Plus Clinical	NP_919304.1:p.Thr830=