Canonical Allele Identifier: CA2250875369
Gene: MYO15A HGNC NCBI

Linked Data

dbSNP Id: rs2046743390

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18159545C>T , CM000679.2:g.18159545C>T GRCh38
NC_000017.10:g.18062859C>T , CM000679.1:g.18062859C>T GRCh37
NC_000017.9:g.18003584C>T NCBI36
NG_011634.1:g.55840C>T
NG_011634.2:g.55840C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642418.1:n.1567+198C>T
ENST00000643693.1:n.1032-61C>T
ENST00000644795.1:c.1022-61C>T ENSP00000495720.1:n.1022-61C>T
ENST00000646782.1:n.1964-61C>T
ENST00000647165.2:c.9230-61C>T MANE Select ENSP00000495481.1:n.9230-61C>T
ENST00000651214.1:n.1734+198C>T
ENST00000205890.9:c.9230-61C>T ENSP00000205890.5:n.9230-61C>T
ENST00000418233.7:c.1022-61C>T ENSP00000408800.3:n.1022-61C>T
ENST00000433411.7:n.364C>T
ENST00000445289.6:n.316+1645C>T
ENST00000556535.5:c.92-61C>T ENSP00000451782.1:n.92-61C>T
ENST00000557190.5:n.131+198C>T
ENST00000557655.5:c.91+198C>T ENSP00000451925.1:n.91+198C>T
ENST00000578472.5:c.92-61C>T ENSP00000467989.1:n.92-61C>T
ENST00000615845.4:c.9230-61C>T ENSP00000481642.1:n.9230-61C>T
NM_016239.3:c.9230-61C>T NP_057323.3:n.9230-61C>T
XM_011523921.1:c.9224-61C>T XP_011522223.1:n.9224-61C>T
XM_017024714.2:c.9170-61C>T XP_016880203.1:n.9170-61C>T
XM_017024715.2:c.9233-61C>T XP_016880204.1:n.9233-61C>T
NM_016239.4:c.9230-61C>T MANE Select NP_057323.3:n.9230-61C>T