Canonical Allele Identifier: CA398633874

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18062622G>T (hg19) ; chr17:g.18159308G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159308G>T , CM000679.2:g.18159308G>T	GRCh38
NC_000017.10:g.18062622G>T , CM000679.1:g.18062622G>T	GRCh37
NC_000017.9:g.18003347G>T	NCBI36
NG_011634.1:g.55603G>T
NG_011634.2:g.55603G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1528G>T
ENST00000643693.1:n.992G>T
ENST00000644795.1:c.982G>T	ENSP00000495720.1:p.Asp328Tyr
ENST00000646782.1:n.1924G>T
ENST00000647165.2:c.9190G>T MANE Select	ENSP00000495481.1:p.Asp3064Tyr
ENST00000651214.1:n.1695G>T
ENST00000205890.9:c.9190G>T	ENSP00000205890.5:p.Asp3064Tyr
ENST00000418233.7:c.982G>T	ENSP00000408800.3:p.Asp328Tyr
ENST00000433411.7:n.127G>T
ENST00000445289.6:n.316+1408G>T
ENST00000556535.5:c.52G>T	ENSP00000451782.1:p.Asp18Tyr
ENST00000557190.5:n.92G>T
ENST00000557655.5:c.52G>T	ENSP00000451925.1:p.Asp18Tyr
ENST00000578472.5:c.52G>T	ENSP00000467989.1:p.Asp18Tyr
ENST00000615845.4:c.9190G>T	ENSP00000481642.1:p.Asp3064Tyr
NM_016239.3:c.9190G>T	NP_057323.3:p.Asp3064Tyr
XM_011523921.1:c.9184G>T	XP_011522223.1:p.Asp3062Tyr
XM_017024714.2:c.9130G>T	XP_016880203.1:p.Asp3044Tyr
XM_017024715.2:c.9193G>T	XP_016880204.1:p.Asp3065Tyr
NM_016239.4:c.9190G>T MANE Select	NP_057323.3:p.Asp3064Tyr