Canonical Allele Identifier: CA398633659

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18062599A>T (hg19) ; chr17:g.18159285A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159285A>T , CM000679.2:g.18159285A>T	GRCh38
NC_000017.10:g.18062599A>T , CM000679.1:g.18062599A>T	GRCh37
NC_000017.9:g.18003324A>T	NCBI36
NG_011634.1:g.55580A>T
NG_011634.2:g.55580A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1505A>T
ENST00000643693.1:n.969A>T
ENST00000644795.1:c.959A>T	ENSP00000495720.1:p.Gln320Leu
ENST00000646782.1:n.1901A>T
ENST00000647165.2:c.9167A>T MANE Select	ENSP00000495481.1:p.Gln3056Leu
ENST00000651214.1:n.1672A>T
ENST00000205890.9:c.9167A>T	ENSP00000205890.5:p.Gln3056Leu
ENST00000418233.7:c.959A>T	ENSP00000408800.3:p.Gln320Leu
ENST00000433411.7:n.104A>T
ENST00000445289.6:n.316+1385A>T
ENST00000556535.5:c.29A>T	ENSP00000451782.1:p.Gln10Leu
ENST00000557190.5:n.69A>T
ENST00000557655.5:c.29A>T	ENSP00000451925.1:p.Gln10Leu
ENST00000578472.5:c.29A>T	ENSP00000467989.1:p.Gln10Leu
ENST00000615845.4:c.9167A>T	ENSP00000481642.1:p.Gln3056Leu
NM_016239.3:c.9167A>T	NP_057323.3:p.Gln3056Leu
XM_011523921.1:c.9161A>T	XP_011522223.1:p.Gln3054Leu
XM_017024714.2:c.9107A>T	XP_016880203.1:p.Gln3036Leu
XM_017024715.2:c.9170A>T	XP_016880204.1:p.Gln3057Leu
NM_016239.4:c.9167A>T MANE Select	NP_057323.3:p.Gln3056Leu