Canonical Allele Identifier: CA2250874654

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159278C= , CM000679.2:g.18159278C=	GRCh38
NC_000017.10:g.18062592C= , CM000679.1:g.18062592C=	GRCh37
NC_000017.9:g.18003317C=	NCBI36
NG_011634.1:g.55573C=
NG_011634.2:g.55573C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1498C=
ENST00000643693.1:n.962C=
ENST00000644795.1:c.952C=	ENSP00000495720.1:p.Pro318=
ENST00000646782.1:n.1894C=
ENST00000647165.2:c.9160C= MANE Select	ENSP00000495481.1:p.Pro3054=
ENST00000651214.1:n.1665C=
ENST00000205890.9:c.9160C=	ENSP00000205890.5:p.Pro3054=
ENST00000418233.7:c.952C=	ENSP00000408800.3:p.Pro318=
ENST00000433411.7:n.97C=
ENST00000445289.6:n.316+1378C=
ENST00000556535.5:c.22C=	ENSP00000451782.1:p.Pro8=
ENST00000557190.5:n.62C=
ENST00000557655.5:c.22C=	ENSP00000451925.1:p.Pro8=
ENST00000578472.5:c.22C=	ENSP00000467989.1:p.Pro8=
ENST00000615845.4:c.9160C=	ENSP00000481642.1:p.Pro3054=
NM_016239.3:c.9160C=	NP_057323.3:p.Pro3054=
XM_011523921.1:c.9154C=	XP_011522223.1:p.Pro3052=
XM_017024714.2:c.9100C=	XP_016880203.1:p.Pro3034=
XM_017024715.2:c.9163C=	XP_016880204.1:p.Pro3055=
NM_016239.4:c.9160C= MANE Select	NP_057323.3:p.Pro3054=