Canonical Allele Identifier: CA2250897992

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18171764G= , CM000679.2:g.18171764G=	GRCh38
NC_000017.10:g.18075078G= , CM000679.1:g.18075078G=	GRCh37
NC_000017.9:g.18015803G=	NCBI36
NG_011634.1:g.68059G=
NG_011634.2:g.68059G=

Transcript Alleles

HGVS	Amino-acid Change
NM_016239.4:c.10209G= MANE Select	NP_057323.3:p.Gln3403=
ENST00000647165.2:c.10209G= MANE Select	ENSP00000495481.1:p.Gln3403=
NM_016239.3:c.10209G=	NP_057323.3:p.Gln3403=
ENST00000205890.9:c.10209G=	ENSP00000205890.5:p.Gln3403=
ENST00000418233.7:c.2001G=	ENSP00000408800.3:p.Gln667=
ENST00000433411.7:n.1659G=
ENST00000445289.6:n.978G=
ENST00000578575.1:c.751G=
ENST00000579848.6:c.629G=	ENSP00000465910.1:p.Ser210=
ENST00000615845.4:c.10209G=	ENSP00000481642.1:p.Gln3403=
ENST00000642418.1:n.2613G=
ENST00000643693.1:n.2151G=
ENST00000644795.1:c.2001G=	ENSP00000495720.1:p.Gln667=
ENST00000646782.1:n.2943G=
ENST00000651214.1:n.2640G=
XM_011523921.1:c.10203G=	XP_011522223.1:p.Gln3401=
XM_017024714.2:c.10149G=	XP_016880203.1:p.Gln3383=
XM_017024715.2:c.10212G=	XP_016880204.1:p.Gln3404=