Canonical Allele Identifier: CA726646647

Gene: MYO15A

Linked Data

• dbSNP Id: rs1331126820
• MyVariant Identifiers: chr17:g.18052726G>T (hg19) ; chr17:g.18149412G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18149412G>T , CM000679.2:g.18149412G>T	GRCh38
NC_000017.10:g.18052726G>T , CM000679.1:g.18052726G>T	GRCh37
NC_000017.9:g.17993451G>T	NCBI36
NG_011634.1:g.45707G>T
NG_011634.2:g.45707G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7117+36G>T MANE Select	ENSP00000495481.1:n.7117+36G>T
ENST00000205890.9:c.7117+36G>T	ENSP00000205890.5:n.7117+36G>T
ENST00000578999.1:n.665G>T
ENST00000615845.4:c.7117+36G>T	ENSP00000481642.1:n.7117+36G>T
NM_016239.3:c.7117+36G>T	NP_057323.3:n.7117+36G>T
XM_011523917.1:c.6792+36G>T	XP_011522219.1:n.6792+36G>T
XM_011523921.1:c.7111+36G>T	XP_011522223.1:n.7111+36G>T
XR_934037.1:n.7451+36G>T
XR_934038.1:n.7404-74G>T
XR_934293.1:n.435-1806C>A
XR_934295.1:n.254-1806C>A
XM_017024714.2:c.7057+36G>T	XP_016880203.1:n.7057+36G>T
XM_017024715.2:c.7120+36G>T	XP_016880204.1:n.7120+36G>T
XR_934293.2:n.378-1806C>A
NM_016239.4:c.7117+36G>T MANE Select	NP_057323.3:n.7117+36G>T