Canonical Allele Identifier: CA498203902

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18062591T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159277T>G , CM000679.2:g.18159277T>G	GRCh38
NC_000017.10:g.18062591T>G , CM000679.1:g.18062591T>G	GRCh37
NC_000017.9:g.18003316T>G	NCBI36
NG_011634.1:g.55572T>G
NG_011634.2:g.55572T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1497T>G
ENST00000643693.1:n.961T>G
ENST00000644795.1:c.951T>G	ENSP00000495720.1:p.Thr317=
ENST00000646782.1:n.1893T>G
ENST00000647165.2:c.9159T>G MANE Select	ENSP00000495481.1:p.Thr3053=
ENST00000651214.1:n.1664T>G
ENST00000205890.9:c.9159T>G	ENSP00000205890.5:p.Thr3053=
ENST00000418233.7:c.951T>G	ENSP00000408800.3:p.Thr317=
ENST00000433411.7:n.96T>G
ENST00000445289.6:n.316+1377T>G
ENST00000556535.5:c.21T>G	ENSP00000451782.1:p.Thr7=
ENST00000557190.5:n.61T>G
ENST00000557655.5:c.21T>G	ENSP00000451925.1:p.Thr7=
ENST00000578472.5:c.21T>G	ENSP00000467989.1:p.Thr7=
ENST00000615845.4:c.9159T>G	ENSP00000481642.1:p.Thr3053=
NM_016239.3:c.9159T>G	NP_057323.3:p.Thr3053=
XM_011523921.1:c.9153T>G	XP_011522223.1:p.Thr3051=
XM_017024714.2:c.9099T>G	XP_016880203.1:p.Thr3033=
XM_017024715.2:c.9162T>G	XP_016880204.1:p.Thr3054=
NM_016239.4:c.9159T>G MANE Select	NP_057323.3:p.Thr3053=