Canonical Allele Identifier: CA8423674

Gene: MYO15A

Linked Data

• ClinVar Variation Id: 2957827
• ClinVar RCV Id: RCV003811490
• dbSNP Id: rs770881392
• ExAC: 17:18030384 G / A
• gnomAD v2: 17-18030384-G-A
• gnomAD v4: 17-18127070-G-A
• MyVariant Identifiers: chr17:g.18030384G>A (hg19) ; chr17:g.18127070G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18127070G>A , CM000679.2:g.18127070G>A	GRCh38
NC_000017.10:g.18030384G>A , CM000679.1:g.18030384G>A	GRCh37
NC_000017.9:g.17971109G>A	NCBI36
NG_011634.1:g.23365G>A
NG_011634.2:g.23365G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647165.2:c.3942-5G>A MANE Select	ENSP00000495481.1:n.3942-5G>A
ENST00000205890.9:c.3942-5G>A	ENSP00000205890.5:n.3942-5G>A
ENST00000615845.4:c.3942-5G>A	ENSP00000481642.1:n.3942-5G>A
NM_016239.3:c.3942-5G>A	NP_057323.3:n.3942-5G>A
XM_011523917.1:c.3942-5G>A	XP_011522219.1:n.3942-5G>A
XM_011523918.1:c.3942-5G>A	XP_011522220.1:n.3942-5G>A
XM_011523919.1:c.3942-5G>A	XP_011522221.1:n.3942-5G>A
XM_011523920.1:c.3942-5G>A	XP_011522222.1:n.3942-5G>A
XM_011523921.1:c.3942-5G>A	XP_011522223.1:n.3942-5G>A
XR_934037.1:n.4601-5G>A
XR_934038.1:n.4601-5G>A
XR_934039.1:n.4601-5G>A
XM_011523918.2:c.3942-5G>A	XP_011522220.1:n.3942-5G>A
XM_017024714.2:c.3942-5G>A	XP_016880203.1:n.3942-5G>A
XM_017024715.2:c.3942-5G>A	XP_016880204.1:n.3942-5G>A
XM_024450780.1:c.3942-5G>A	XP_024306548.1:n.3942-5G>A
XM_024450781.1:c.3942-5G>A	XP_024306549.1:n.3942-5G>A
XM_024450782.1:c.3942-5G>A	XP_024306550.1:n.3942-5G>A
XR_934039.2:n.4640-5G>A
NM_016239.4:c.3942-5G>A MANE Select	NP_057323.3:n.3942-5G>A