Canonical Allele Identifier: CA625044568

Gene: MYO15A

Linked Data

• dbSNP Id: rs1408194107
• gnomAD v2: 17-18057416-C-T
• gnomAD v4: 17-18154102-C-T
• MyVariant Identifiers: chr17:g.18057416C>T (hg19) ; chr17:g.18154102C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18154102C>T , CM000679.2:g.18154102C>T	GRCh38
NC_000017.10:g.18057416C>T , CM000679.1:g.18057416C>T	GRCh37
NC_000017.9:g.17998141C>T	NCBI36
NG_011634.1:g.50397C>T
NG_011634.2:g.50397C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644795.1:c.-120-29C>T	ENSP00000495720.1:n.-120-29C>T
ENST00000646782.1:n.244-29C>T
ENST00000647165.2:c.8089-29C>T MANE Select	ENSP00000495481.1:n.8089-29C>T
ENST00000651214.1:n.235-29C>T
ENST00000205890.9:c.8089-29C>T	ENSP00000205890.5:n.8089-29C>T
ENST00000418233.7:c.-120-29C>T	ENSP00000408800.3:n.-120-29C>T
ENST00000445289.6:n.49C>T
ENST00000536811.5:n.49C>T
ENST00000585180.1:c.-149C>T	ENSP00000464462.1:n.-149C>T
ENST00000615845.4:c.8089-29C>T	ENSP00000481642.1:n.8089-29C>T
NM_016239.3:c.8089-29C>T	NP_057323.3:n.8089-29C>T
XM_011523921.1:c.8083-29C>T	XP_011522223.1:n.8083-29C>T
XM_017024714.2:c.8029-29C>T	XP_016880203.1:n.8029-29C>T
XM_017024715.2:c.8092-29C>T	XP_016880204.1:n.8092-29C>T
XR_001752809.1:n.297+38G>A
XR_001752810.1:n.297+38G>A
NM_016239.4:c.8089-29C>T MANE Select	NP_057323.3:n.8089-29C>T