Canonical Allele Identifier: CA656491904

Gene: MYO15A

Linked Data

• COSMIC: COSN20078723

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159359G>A , CM000679.2:g.18159359G>A	GRCh38
NC_000017.10:g.18062673G>A , CM000679.1:g.18062673G>A	GRCh37
NC_000017.9:g.18003398G>A	NCBI36
NG_011634.1:g.55654G>A
NG_011634.2:g.55654G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1567+12G>A
ENST00000643693.1:n.1031+12G>A
ENST00000644795.1:c.1021+12G>A	ENSP00000495720.1:n.1021+12G>A
ENST00000646782.1:n.1963+12G>A
ENST00000647165.2:c.9229+12G>A MANE Select	ENSP00000495481.1:n.9229+12G>A
ENST00000651214.1:n.1734+12G>A
ENST00000205890.9:c.9229+12G>A	ENSP00000205890.5:n.9229+12G>A
ENST00000418233.7:c.1021+12G>A	ENSP00000408800.3:n.1021+12G>A
ENST00000433411.7:n.178G>A
ENST00000445289.6:n.316+1459G>A
ENST00000556535.5:c.91+12G>A	ENSP00000451782.1:n.91+12G>A
ENST00000557190.5:n.131+12G>A
ENST00000557655.5:c.91+12G>A	ENSP00000451925.1:n.91+12G>A
ENST00000578472.5:c.91+12G>A	ENSP00000467989.1:n.91+12G>A
ENST00000615845.4:c.9229+12G>A	ENSP00000481642.1:n.9229+12G>A
NM_016239.3:c.9229+12G>A	NP_057323.3:n.9229+12G>A
XM_011523921.1:c.9223+12G>A	XP_011522223.1:n.9223+12G>A
XM_017024714.2:c.9169+12G>A	XP_016880203.1:n.9169+12G>A
XM_017024715.2:c.9232+12G>A	XP_016880204.1:n.9232+12G>A
NM_016239.4:c.9229+12G>A MANE Select	NP_057323.3:n.9229+12G>A