Canonical Allele Identifier: CA2250856103

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18154190G= , CM000679.2:g.18154190G=	GRCh38
NC_000017.10:g.18057504G= , CM000679.1:g.18057504G=	GRCh37
NC_000017.9:g.17998229G=	NCBI36
NG_011634.1:g.50485G=
NG_011634.2:g.50485G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644795.1:c.-61G=	ENSP00000495720.1:n.-61G=
ENST00000646782.1:n.303G=
ENST00000647165.2:c.8148G= MANE Select	ENSP00000495481.1:p.Gln2716=
ENST00000651214.1:n.294G=
ENST00000205890.9:c.8148G=	ENSP00000205890.5:p.Gln2716=
ENST00000418233.7:c.-61G=	ENSP00000408800.3:n.-61G=
ENST00000445289.6:n.137G=
ENST00000536811.5:n.137G=
ENST00000585180.1:c.-61G=	ENSP00000464462.1:n.-61G=
ENST00000615845.4:c.8148G=	ENSP00000481642.1:p.Gln2716=
NM_016239.3:c.8148G=	NP_057323.3:p.Gln2716=
XM_011523921.1:c.8142G=	XP_011522223.1:p.Gln2714=
XM_017024714.2:c.8088G=	XP_016880203.1:p.Gln2696=
XM_017024715.2:c.8151G=	XP_016880204.1:p.Gln2717=
XR_001752809.1:n.247C=
XR_001752810.1:n.247C=
NM_016239.4:c.8148G= MANE Select	NP_057323.3:p.Gln2716=