Canonical Allele Identifier: CA398634042

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18062643G>A (hg19) ; chr17:g.18159329G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159329G>A , CM000679.2:g.18159329G>A	GRCh38
NC_000017.10:g.18062643G>A , CM000679.1:g.18062643G>A	GRCh37
NC_000017.9:g.18003368G>A	NCBI36
NG_011634.1:g.55624G>A
NG_011634.2:g.55624G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1549G>A
ENST00000643693.1:n.1013G>A
ENST00000644795.1:c.1003G>A	ENSP00000495720.1:p.Ala335Thr
ENST00000646782.1:n.1945G>A
ENST00000647165.2:c.9211G>A MANE Select	ENSP00000495481.1:p.Ala3071Thr
ENST00000651214.1:n.1716G>A
ENST00000205890.9:c.9211G>A	ENSP00000205890.5:p.Ala3071Thr
ENST00000418233.7:c.1003G>A	ENSP00000408800.3:p.Ala335Thr
ENST00000433411.7:n.148G>A
ENST00000445289.6:n.316+1429G>A
ENST00000556535.5:c.73G>A	ENSP00000451782.1:p.Ala25Thr
ENST00000557190.5:n.113G>A
ENST00000557655.5:c.73G>A	ENSP00000451925.1:p.Ala25Thr
ENST00000578472.5:c.73G>A	ENSP00000467989.1:p.Ala25Thr
ENST00000615845.4:c.9211G>A	ENSP00000481642.1:p.Ala3071Thr
NM_016239.3:c.9211G>A	NP_057323.3:p.Ala3071Thr
XM_011523921.1:c.9205G>A	XP_011522223.1:p.Ala3069Thr
XM_017024714.2:c.9151G>A	XP_016880203.1:p.Ala3051Thr
XM_017024715.2:c.9214G>A	XP_016880204.1:p.Ala3072Thr
NM_016239.4:c.9211G>A MANE Select	NP_057323.3:p.Ala3071Thr