Canonical Allele Identifier: CA2250874931

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159328G= , CM000679.2:g.18159328G=	GRCh38
NC_000017.10:g.18062642G= , CM000679.1:g.18062642G=	GRCh37
NC_000017.9:g.18003367G=	NCBI36
NG_011634.1:g.55623G=
NG_011634.2:g.55623G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1548G=
ENST00000643693.1:n.1012G=
ENST00000644795.1:c.1002G=	ENSP00000495720.1:p.Met334=
ENST00000646782.1:n.1944G=
ENST00000647165.2:c.9210G= MANE Select	ENSP00000495481.1:p.Met3070=
ENST00000651214.1:n.1715G=
ENST00000205890.9:c.9210G=	ENSP00000205890.5:p.Met3070=
ENST00000418233.7:c.1002G=	ENSP00000408800.3:p.Met334=
ENST00000433411.7:n.147G=
ENST00000445289.6:n.316+1428G=
ENST00000556535.5:c.72G=	ENSP00000451782.1:p.Met24=
ENST00000557190.5:n.112G=
ENST00000557655.5:c.72G=	ENSP00000451925.1:p.Met24=
ENST00000578472.5:c.72G=	ENSP00000467989.1:p.Met24=
ENST00000615845.4:c.9210G=	ENSP00000481642.1:p.Met3070=
NM_016239.3:c.9210G=	NP_057323.3:p.Met3070=
XM_011523921.1:c.9204G=	XP_011522223.1:p.Met3068=
XM_017024714.2:c.9150G=	XP_016880203.1:p.Met3050=
XM_017024715.2:c.9213G=	XP_016880204.1:p.Met3071=
NM_016239.4:c.9210G= MANE Select	NP_057323.3:p.Met3070=