Canonical Allele Identifier: CA2250852156

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150353G= , CM000679.2:g.18150353G=	GRCh38
NC_000017.10:g.18053667G= , CM000679.1:g.18053667G=	GRCh37
NC_000017.9:g.17994392G=	NCBI36
NG_011634.1:g.46648G=
NG_011634.2:g.46648G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7213-76G= MANE Select	ENSP00000495481.1:n.7213-76G=
ENST00000205890.9:c.7213-76G=	ENSP00000205890.5:n.7213-76G=
ENST00000615845.4:c.7213-76G=	ENSP00000481642.1:n.7213-76G=
NM_016239.3:c.7213-76G=	NP_057323.3:n.7213-76G=
XM_011523917.1:c.6888-76G=	XP_011522219.1:n.6888-76G=
XM_011523921.1:c.7207-76G=	XP_011522223.1:n.7207-76G=
XR_934037.1:n.7547-76G=
XR_934038.1:n.7499-76G=
XR_934293.1:n.434+1250C=
XR_934294.1:n.435-580C=
XR_934295.1:n.253+1250C=
XM_017024714.2:c.7153-76G=	XP_016880203.1:n.7153-76G=
XM_017024715.2:c.7216-76G=	XP_016880204.1:n.7216-76G=
XR_934293.2:n.377+1250C=
XR_934294.2:n.378-580C=
NM_016239.4:c.7213-76G= MANE Select	NP_057323.3:n.7213-76G=