Canonical Allele Identifier: CA501765306

Gene: OTOP2 USH1G

Linked Data

• MyVariant Identifiers: chr17:g.72919049G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74922954G>C , CM000679.2:g.74922954G>C	GRCh38
NC_000017.10:g.72919049G>C , CM000679.1:g.72919049G>C	GRCh37
NC_000017.9:g.70430644G>C	NCBI36
NG_007882.1:g.5303C>G
NG_033062.1:g.3680G>C
NG_007882.2:g.5310C>G
NG_033062.2:g.3680G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000580223.2:c.-311G>C (OTOP2)	ENSP00000463837.2:n.-311G>C
ENST00000614341.5:c.120C>G (USH1G) MANE Select	ENSP00000480279.1:p.Ala40=
ENST00000579243.1:c.120C>G (USH1G)	ENSP00000462568.1:p.Ala40=
ENST00000614341.4:c.120C>G (USH1G)	ENSP00000480279.1:p.Ala40=
NM_001282489.2:c.-137C>G (USH1G)	NP_001269418.1:n.-137C>G
NM_173477.4:c.120C>G (USH1G)	NP_775748.2:p.Ala40=
NM_173477.5:c.120C>G (USH1G) MANE Select	NP_775748.2:p.Ala40=
NM_001282489.3:c.-137C>G (USH1G)	NP_001269418.1:n.-137C>G