Canonical Allele Identifier: CA8425002

Gene: MYO15A

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644795.1:c.-159T>C	ENSP00000495720.1:n.-159T>C
ENST00000646782.1:n.205T>C
ENST00000647165.2:c.8050T>C MANE Select	ENSP00000495481.1:p.Tyr2684His
ENST00000651214.1:n.196T>C
ENST00000205890.9:c.8050T>C	ENSP00000205890.5:p.Tyr2684His
ENST00000418233.7:c.-159T>C	ENSP00000408800.3:n.-159T>C
ENST00000615845.4:c.8050T>C	ENSP00000481642.1:p.Tyr2684His
NM_016239.3:c.8050T>C	NP_057323.3:p.Tyr2684His
XM_011523921.1:c.8044T>C	XP_011522223.1:p.Tyr2682His
XM_017024714.2:c.7990T>C	XP_016880203.1:p.Tyr2664His
XM_017024715.2:c.8053T>C	XP_016880204.1:p.Tyr2685His
XR_001752809.1:n.324A>G
XR_001752810.1:n.367A>G
NM_016239.4:c.8050T>C MANE Select	NP_057323.3:p.Tyr2684His