Canonical Allele Identifier: CA2250850358

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18146034C= , CM000679.2:g.18146034C=	GRCh38
NC_000017.10:g.18049348C= , CM000679.1:g.18049348C=	GRCh37
NC_000017.9:g.17990073C=	NCBI36
NG_011634.1:g.42329C=
NG_011634.2:g.42329C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6436C= MANE Select	ENSP00000495481.1:p.Arg2146=
ENST00000205890.9:c.6436C=	ENSP00000205890.5:p.Arg2146=
ENST00000578999.1:n.21C=
ENST00000615845.4:c.6436C=	ENSP00000481642.1:p.Arg2146=
NM_016239.3:c.6436C=	NP_057323.3:p.Arg2146=
XM_011523917.1:c.6376C=	XP_011522219.1:p.Arg2126=
XM_011523918.1:c.6342+34C=	XP_011522220.1:n.6342+34C=
XM_011523921.1:c.6430C=	XP_011522223.1:p.Arg2144=
XR_934037.1:n.7035C=
XR_934038.1:n.7035C=
XM_011523918.2:c.6342+34C=	XP_011522220.1:n.6342+34C=
XM_017024714.2:c.6376C=	XP_016880203.1:p.Arg2126=
XM_017024715.2:c.6439C=	XP_016880204.1:p.Arg2147=
XM_024450781.1:c.6213+1442C=	XP_024306549.1:n.6213+1442C=
NM_016239.4:c.6436C= MANE Select	NP_057323.3:p.Arg2146=