Canonical Allele Identifier: CA398634021

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18062641T>A (hg19) ; chr17:g.18159327T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18159327T>A , CM000679.2:g.18159327T>A	GRCh38
NC_000017.10:g.18062641T>A , CM000679.1:g.18062641T>A	GRCh37
NC_000017.9:g.18003366T>A	NCBI36
NG_011634.1:g.55622T>A
NG_011634.2:g.55622T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.1547T>A
ENST00000643693.1:n.1011T>A
ENST00000644795.1:c.1001T>A	ENSP00000495720.1:p.Met334Lys
ENST00000646782.1:n.1943T>A
ENST00000647165.2:c.9209T>A MANE Select	ENSP00000495481.1:p.Met3070Lys
ENST00000651214.1:n.1714T>A
ENST00000205890.9:c.9209T>A	ENSP00000205890.5:p.Met3070Lys
ENST00000418233.7:c.1001T>A	ENSP00000408800.3:p.Met334Lys
ENST00000433411.7:n.146T>A
ENST00000445289.6:n.316+1427T>A
ENST00000556535.5:c.71T>A	ENSP00000451782.1:p.Met24Lys
ENST00000557190.5:n.111T>A
ENST00000557655.5:c.71T>A	ENSP00000451925.1:p.Met24Lys
ENST00000578472.5:c.71T>A	ENSP00000467989.1:p.Met24Lys
ENST00000615845.4:c.9209T>A	ENSP00000481642.1:p.Met3070Lys
NM_016239.3:c.9209T>A	NP_057323.3:p.Met3070Lys
XM_011523921.1:c.9203T>A	XP_011522223.1:p.Met3068Lys
XM_017024714.2:c.9149T>A	XP_016880203.1:p.Met3050Lys
XM_017024715.2:c.9212T>A	XP_016880204.1:p.Met3071Lys
NM_016239.4:c.9209T>A MANE Select	NP_057323.3:p.Met3070Lys