Canonical Allele Identifier: CA398624586

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18153853A>G , CM000679.2:g.18153853A>G	GRCh38
NC_000017.10:g.18057167A>G , CM000679.1:g.18057167A>G	GRCh37
NC_000017.9:g.17997892A>G	NCBI36
NG_011634.1:g.50148A>G
NG_011634.2:g.50148A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016239.4:c.8045A>G MANE Select	NP_057323.3:p.Tyr2682Cys
ENST00000647165.2:c.8045A>G MANE Select	ENSP00000495481.1:p.Tyr2682Cys
NM_016239.3:c.8045A>G	NP_057323.3:p.Tyr2682Cys
ENST00000205890.9:c.8045A>G	ENSP00000205890.5:p.Tyr2682Cys
ENST00000418233.7:c.-164A>G	ENSP00000408800.3:n.-164A>G
ENST00000615845.4:c.8045A>G	ENSP00000481642.1:p.Tyr2682Cys
ENST00000644795.1:c.-164A>G	ENSP00000495720.1:n.-164A>G
ENST00000646782.1:n.200A>G
ENST00000651214.1:n.191A>G
XM_011523921.1:c.8039A>G	XP_011522223.1:p.Tyr2680Cys
XM_017024714.2:c.7985A>G	XP_016880203.1:p.Tyr2662Cys
XM_017024715.2:c.8048A>G	XP_016880204.1:p.Tyr2683Cys
XR_001752809.1:n.329T>C
XR_001752810.1:n.372T>C