Canonical Allele Identifier: CA2250874512

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159235T= , CM000679.2:g.18159235T=	GRCh38
NC_000017.10:g.18062549T= , CM000679.1:g.18062549T=	GRCh37
NC_000017.9:g.18003274T=	NCBI36
NG_011634.1:g.55530T=
NG_011634.2:g.55530T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1495-40T=
ENST00000643693.1:n.959-40T=
ENST00000644795.1:c.949-40T=	ENSP00000495720.1:n.949-40T=
ENST00000646782.1:n.1891-40T=
ENST00000647165.2:c.9157-40T= MANE Select	ENSP00000495481.1:n.9157-40T=
ENST00000651214.1:n.1662-40T=
ENST00000205890.9:c.9157-40T=	ENSP00000205890.5:n.9157-40T=
ENST00000418233.7:c.949-40T=	ENSP00000408800.3:n.949-40T=
ENST00000433411.7:n.94-40T=
ENST00000445289.6:n.316+1335T=
ENST00000556535.5:c.19-40T=	ENSP00000451782.1:n.19-40T=
ENST00000557190.5:n.59-40T=
ENST00000557655.5:c.19-40T=	ENSP00000451925.1:n.19-40T=
ENST00000578472.5:c.19-40T=	ENSP00000467989.1:n.19-40T=
ENST00000615845.4:c.9157-40T=	ENSP00000481642.1:n.9157-40T=
NM_016239.3:c.9157-40T=	NP_057323.3:n.9157-40T=
XM_011523921.1:c.9151-40T=	XP_011522223.1:n.9151-40T=
XM_017024714.2:c.9097-40T=	XP_016880203.1:n.9097-40T=
XM_017024715.2:c.9160-40T=	XP_016880204.1:n.9160-40T=
NM_016239.4:c.9157-40T= MANE Select	NP_057323.3:n.9157-40T=