Canonical Allele Identifier: CA261769

Gene: MYO15A

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18149265dup , CM000679.2:g.18149265dup	GRCh38
NC_000017.10:g.18052579dup , CM000679.1:g.18052579dup	GRCh37
NC_000017.9:g.17993304dup	NCBI36
NG_011634.1:g.45560dup
NG_011634.2:g.45560dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7006dup MANE Select	ENSP00000495481.1:p.Gln2336ProfsTer11
ENST00000205890.9:c.7006dup	ENSP00000205890.5:p.Gln2336ProfsTer11
ENST00000578999.1:n.518dup
ENST00000615845.4:c.7006dup	ENSP00000481642.1:p.Gln2336ProfsTer11
NM_016239.3:c.7006dup	NP_057323.3:p.Gln2336ProfsTer11
XM_011523917.1:c.6681dup	XP_011522219.1:p.Ser2228GlnfsTer?
XM_011523921.1:c.7000dup	XP_011522223.1:p.Gln2334ProfsTer11
XR_934037.1:n.7340dup
XR_934038.1:n.7340dup
XR_934293.1:n.435-1656dup
XR_934295.1:n.254-1656dup
XM_017024714.2:c.6946dup	XP_016880203.1:p.Gln2316ProfsTer11
XM_017024715.2:c.7009dup	XP_016880204.1:p.Gln2337ProfsTer11
XR_934293.2:n.378-1656dup
NM_016239.4:c.7006dup MANE Select	NP_057323.3:p.Gln2336ProfsTer11