Canonical Allele Identifier: CA2250874940

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159334C= , CM000679.2:g.18159334C=	GRCh38
NC_000017.10:g.18062648C= , CM000679.1:g.18062648C=	GRCh37
NC_000017.9:g.18003373C=	NCBI36
NG_011634.1:g.55629C=
NG_011634.2:g.55629C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1554C=
ENST00000643693.1:n.1018C=
ENST00000644795.1:c.1008C=	ENSP00000495720.1:p.Thr336=
ENST00000646782.1:n.1950C=
ENST00000647165.2:c.9216C= MANE Select	ENSP00000495481.1:p.Thr3072=
ENST00000651214.1:n.1721C=
ENST00000205890.9:c.9216C=	ENSP00000205890.5:p.Thr3072=
ENST00000418233.7:c.1008C=	ENSP00000408800.3:p.Thr336=
ENST00000433411.7:n.153C=
ENST00000445289.6:n.316+1434C=
ENST00000556535.5:c.78C=	ENSP00000451782.1:p.Thr26=
ENST00000557190.5:n.118C=
ENST00000557655.5:c.78C=	ENSP00000451925.1:p.Thr26=
ENST00000578472.5:c.78C=	ENSP00000467989.1:p.Thr26=
ENST00000615845.4:c.9216C=	ENSP00000481642.1:p.Thr3072=
NM_016239.3:c.9216C=	NP_057323.3:p.Thr3072=
XM_011523921.1:c.9210C=	XP_011522223.1:p.Thr3070=
XM_017024714.2:c.9156C=	XP_016880203.1:p.Thr3052=
XM_017024715.2:c.9219C=	XP_016880204.1:p.Thr3073=
NM_016239.4:c.9216C= MANE Select	NP_057323.3:p.Thr3072=