Canonical Allele Identifier: CA2250850355

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18146026A= , CM000679.2:g.18146026A=	GRCh38
NC_000017.10:g.18049340A= , CM000679.1:g.18049340A=	GRCh37
NC_000017.9:g.17990065A=	NCBI36
NG_011634.1:g.42321A=
NG_011634.2:g.42321A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6428A= MANE Select	ENSP00000495481.1:p.Asn2143=
ENST00000205890.9:c.6428A=	ENSP00000205890.5:p.Asn2143=
ENST00000578999.1:n.13A=
ENST00000615845.4:c.6428A=	ENSP00000481642.1:p.Asn2143=
NM_016239.3:c.6428A=	NP_057323.3:p.Asn2143=
XM_011523917.1:c.6368A=	XP_011522219.1:p.Asn2123=
XM_011523918.1:c.6342+26A=	XP_011522220.1:n.6342+26A=
XM_011523921.1:c.6422A=	XP_011522223.1:p.Asn2141=
XR_934037.1:n.7027A=
XR_934038.1:n.7027A=
XM_011523918.2:c.6342+26A=	XP_011522220.1:n.6342+26A=
XM_017024714.2:c.6368A=	XP_016880203.1:p.Asn2123=
XM_017024715.2:c.6431A=	XP_016880204.1:p.Asn2144=
XM_024450781.1:c.6213+1434A=	XP_024306549.1:n.6213+1434A=
NM_016239.4:c.6428A= MANE Select	NP_057323.3:p.Asn2143=