Canonical Allele Identifier: CA2250852150

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150343G= , CM000679.2:g.18150343G=	GRCh38
NC_000017.10:g.18053657G= , CM000679.1:g.18053657G=	GRCh37
NC_000017.9:g.17994382G=	NCBI36
NG_011634.1:g.46638G=
NG_011634.2:g.46638G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647165.2:c.7213-86G= MANE Select	ENSP00000495481.1:n.7213-86G=
ENST00000205890.9:c.7213-86G=	ENSP00000205890.5:n.7213-86G=
ENST00000615845.4:c.7213-86G=	ENSP00000481642.1:n.7213-86G=
NM_016239.3:c.7213-86G=	NP_057323.3:n.7213-86G=
XM_011523917.1:c.6888-86G=	XP_011522219.1:n.6888-86G=
XM_011523921.1:c.7207-86G=	XP_011522223.1:n.7207-86G=
XR_934037.1:n.7547-86G=
XR_934038.1:n.7499-86G=
XR_934293.1:n.434+1260C=
XR_934294.1:n.435-570C=
XR_934295.1:n.253+1260C=
XM_017024714.2:c.7153-86G=	XP_016880203.1:n.7153-86G=
XM_017024715.2:c.7216-86G=	XP_016880204.1:n.7216-86G=
XR_934293.2:n.377+1260C=
XR_934294.2:n.378-570C=
NM_016239.4:c.7213-86G= MANE Select	NP_057323.3:n.7213-86G=