Canonical Allele Identifier: CA2250856134

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18154207C= , CM000679.2:g.18154207C=	GRCh38
NC_000017.10:g.18057521C= , CM000679.1:g.18057521C=	GRCh37
NC_000017.9:g.17998246C=	NCBI36
NG_011634.1:g.50502C=
NG_011634.2:g.50502C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644795.1:c.-61+17C=	ENSP00000495720.1:n.-61+17C=
ENST00000646782.1:n.303+17C=
ENST00000647165.2:c.8148+17C= MANE Select	ENSP00000495481.1:n.8148+17C=
ENST00000651214.1:n.294+17C=
ENST00000205890.9:c.8148+17C=	ENSP00000205890.5:n.8148+17C=
ENST00000418233.7:c.-61+17C=	ENSP00000408800.3:n.-61+17C=
ENST00000445289.6:n.137+17C=
ENST00000536811.5:n.137+17C=
ENST00000585180.1:c.-61+17C=	ENSP00000464462.1:n.-61+17C=
ENST00000615845.4:c.8148+17C=	ENSP00000481642.1:n.8148+17C=
NM_016239.3:c.8148+17C=	NP_057323.3:n.8148+17C=
XM_011523921.1:c.8142+17C=	XP_011522223.1:n.8142+17C=
XM_017024714.2:c.8088+17C=	XP_016880203.1:n.8088+17C=
XM_017024715.2:c.8151+17C=	XP_016880204.1:n.8151+17C=
XR_001752809.1:n.230G=
XR_001752810.1:n.230G=
NM_016239.4:c.8148+17C= MANE Select	NP_057323.3:n.8148+17C=