Canonical Allele Identifier: CA2250850357

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18146033G= , CM000679.2:g.18146033G=	GRCh38
NC_000017.10:g.18049347G= , CM000679.1:g.18049347G=	GRCh37
NC_000017.9:g.17990072G=	NCBI36
NG_011634.1:g.42328G=
NG_011634.2:g.42328G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6435G= MANE Select	ENSP00000495481.1:p.Glu2145=
ENST00000205890.9:c.6435G=	ENSP00000205890.5:p.Glu2145=
ENST00000578999.1:n.20G=
ENST00000615845.4:c.6435G=	ENSP00000481642.1:p.Glu2145=
NM_016239.3:c.6435G=	NP_057323.3:p.Glu2145=
XM_011523917.1:c.6375G=	XP_011522219.1:p.Glu2125=
XM_011523918.1:c.6342+33G=	XP_011522220.1:n.6342+33G=
XM_011523921.1:c.6429G=	XP_011522223.1:p.Glu2143=
XR_934037.1:n.7034G=
XR_934038.1:n.7034G=
XM_011523918.2:c.6342+33G=	XP_011522220.1:n.6342+33G=
XM_017024714.2:c.6375G=	XP_016880203.1:p.Glu2125=
XM_017024715.2:c.6438G=	XP_016880204.1:p.Glu2146=
XM_024450781.1:c.6213+1441G=	XP_024306549.1:n.6213+1441G=
NM_016239.4:c.6435G= MANE Select	NP_057323.3:p.Glu2145=