Canonical Allele Identifier: CA2250851774

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18149476_18149477delinsTC , CM000679.2:g.18149476_18149477delinsTC	GRCh38
NC_000017.10:g.18052790_18052791delinsTC , CM000679.1:g.18052790_18052791delinsTC	GRCh37
NC_000017.9:g.17993515_17993516delinsTC	NCBI36
NG_011634.1:g.45771_45772delinsTC
NG_011634.2:g.45771_45772delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7118-10_7118-9delinsTC MANE Select	ENSP00000495481.1:n.7118-10_7118-9delinsTC
ENST00000205890.9:c.7118-10_7118-9delinsTC	ENSP00000205890.5:n.7118-10_7118-9delinsTC
ENST00000578999.1:n.729_730delinsTC
ENST00000615845.4:c.7118-10_7118-9delinsTC	ENSP00000481642.1:n.7118-10_7118-9delinsTC
NM_016239.3:c.7118-10_7118-9delinsTC	NP_057323.3:n.7118-10_7118-9delinsTC
XM_011523917.1:c.6793-10_6793-9delinsTC	XP_011522219.1:n.6793-10_6793-9delinsTC
XM_011523921.1:c.7112-10_7112-9delinsTC	XP_011522223.1:n.7112-10_7112-9delinsTC
XR_934037.1:n.7452-10_7452-9delinsTC
XR_934038.1:n.7404-10_7404-9delinsTC
XR_934293.1:n.435-1871_435-1870delinsGA
XR_934295.1:n.254-1871_254-1870delinsGA
XM_017024714.2:c.7058-10_7058-9delinsTC	XP_016880203.1:n.7058-10_7058-9delinsTC
XM_017024715.2:c.7121-10_7121-9delinsTC	XP_016880204.1:n.7121-10_7121-9delinsTC
XR_934293.2:n.378-1871_378-1870delinsGA
NM_016239.4:c.7118-10_7118-9delinsTC MANE Select	NP_057323.3:n.7118-10_7118-9delinsTC