Canonical Allele Identifier: CA398624759
Gene: MYO15A HGNC NCBI

Linked Data

dbSNP Id: rs2046628413
gnomAD v4: 17-18153873-T-C
MyVariant Identifiers: chr17:g.18057187T>C (hg19) chr17:g.18153873T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.18153873T>C , CM000679.2:g.18153873T>C GRCh38
NC_000017.10:g.18057187T>C , CM000679.1:g.18057187T>C GRCh37
NC_000017.9:g.17997912T>C NCBI36
NG_011634.1:g.50168T>C
NG_011634.2:g.50168T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644795.1:c.-144T>C ENSP00000495720.1:n.-144T>C
ENST00000646782.1:n.220T>C
ENST00000647165.2:c.8065T>C MANE Select ENSP00000495481.1:p.Trp2689Arg
ENST00000651214.1:n.211T>C
ENST00000205890.9:c.8065T>C ENSP00000205890.5:p.Trp2689Arg
ENST00000418233.7:c.-144T>C ENSP00000408800.3:n.-144T>C
ENST00000615845.4:c.8065T>C ENSP00000481642.1:p.Trp2689Arg
NM_016239.3:c.8065T>C NP_057323.3:p.Trp2689Arg
XM_011523921.1:c.8059T>C XP_011522223.1:p.Trp2687Arg
XM_017024714.2:c.8005T>C XP_016880203.1:p.Trp2669Arg
XM_017024715.2:c.8068T>C XP_016880204.1:p.Trp2690Arg
XR_001752809.1:n.309A>G
XR_001752810.1:n.352A>G
NM_016239.4:c.8065T>C MANE Select NP_057323.3:p.Trp2689Arg
Search 100 bp 5'
Search 100 bp 3'