Canonical Allele Identifier: CA398624617

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18153858T>A , CM000679.2:g.18153858T>A	GRCh38
NC_000017.10:g.18057172T>A , CM000679.1:g.18057172T>A	GRCh37
NC_000017.9:g.17997897T>A	NCBI36
NG_011634.1:g.50153T>A
NG_011634.2:g.50153T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016239.4:c.8050T>A MANE Select	NP_057323.3:p.Tyr2684Asn
ENST00000647165.2:c.8050T>A MANE Select	ENSP00000495481.1:p.Tyr2684Asn
NM_016239.3:c.8050T>A	NP_057323.3:p.Tyr2684Asn
ENST00000205890.9:c.8050T>A	ENSP00000205890.5:p.Tyr2684Asn
ENST00000418233.7:c.-159T>A	ENSP00000408800.3:n.-159T>A
ENST00000615845.4:c.8050T>A	ENSP00000481642.1:p.Tyr2684Asn
ENST00000644795.1:c.-159T>A	ENSP00000495720.1:n.-159T>A
ENST00000646782.1:n.205T>A
ENST00000651214.1:n.196T>A
XM_011523921.1:c.8044T>A	XP_011522223.1:p.Tyr2682Asn
XM_017024714.2:c.7990T>A	XP_016880203.1:p.Tyr2664Asn
XM_017024715.2:c.8053T>A	XP_016880204.1:p.Tyr2685Asn
XR_001752809.1:n.324A>T
XR_001752810.1:n.367A>T