Canonical Allele Identifier: CA398634099

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18062649G>T (hg19) ; chr17:g.18159335G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159335G>T , CM000679.2:g.18159335G>T	GRCh38
NC_000017.10:g.18062649G>T , CM000679.1:g.18062649G>T	GRCh37
NC_000017.9:g.18003374G>T	NCBI36
NG_011634.1:g.55630G>T
NG_011634.2:g.55630G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1555G>T
ENST00000643693.1:n.1019G>T
ENST00000644795.1:c.1009G>T	ENSP00000495720.1:p.Asp337Tyr
ENST00000646782.1:n.1951G>T
ENST00000647165.2:c.9217G>T MANE Select	ENSP00000495481.1:p.Asp3073Tyr
ENST00000651214.1:n.1722G>T
ENST00000205890.9:c.9217G>T	ENSP00000205890.5:p.Asp3073Tyr
ENST00000418233.7:c.1009G>T	ENSP00000408800.3:p.Asp337Tyr
ENST00000433411.7:n.154G>T
ENST00000445289.6:n.316+1435G>T
ENST00000556535.5:c.79G>T	ENSP00000451782.1:p.Asp27Tyr
ENST00000557190.5:n.119G>T
ENST00000557655.5:c.79G>T	ENSP00000451925.1:p.Asp27Tyr
ENST00000578472.5:c.79G>T	ENSP00000467989.1:p.Asp27Tyr
ENST00000615845.4:c.9217G>T	ENSP00000481642.1:p.Asp3073Tyr
NM_016239.3:c.9217G>T	NP_057323.3:p.Asp3073Tyr
XM_011523921.1:c.9211G>T	XP_011522223.1:p.Asp3071Tyr
XM_017024714.2:c.9157G>T	XP_016880203.1:p.Asp3053Tyr
XM_017024715.2:c.9220G>T	XP_016880204.1:p.Asp3074Tyr
NM_016239.4:c.9217G>T MANE Select	NP_057323.3:p.Asp3073Tyr