Canonical Allele Identifier: CA10645001

Gene: MYO15A

Linked Data

• ClinVar Variation Id: 322104
• ClinVar RCV Id: RCV000329622
• dbSNP Id: rs760728232
• gnomAD v2: 17-18021942-T-A
• gnomAD v3: 17-18118628-T-A
• gnomAD v4: 17-18118628-T-A
• MyVariant Identifiers: chr17:g.18021942T>A (hg19) ; chr17:g.18118628T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18118628T>A , CM000679.2:g.18118628T>A	GRCh38
NC_000017.10:g.18021942T>A , CM000679.1:g.18021942T>A	GRCh37
NC_000017.9:g.17962667T>A	NCBI36
NG_011634.1:g.14923T>A
NG_011634.2:g.14923T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.-173T>A MANE Select	ENSP00000495481.1:n.-173T>A
ENST00000205890.9:c.-173T>A	ENSP00000205890.5:n.-173T>A
ENST00000615845.4:c.-173T>A	ENSP00000481642.1:n.-173T>A
NM_016239.3:c.-173T>A	NP_057323.3:n.-173T>A
XM_011523917.1:c.-173T>A	XP_011522219.1:n.-173T>A
XM_011523918.1:c.-173T>A	XP_011522220.1:n.-173T>A
XM_011523919.1:c.-173T>A	XP_011522221.1:n.-173T>A
XM_011523920.1:c.-173T>A	XP_011522222.1:n.-173T>A
XM_011523921.1:c.-173T>A	XP_011522223.1:n.-173T>A
XR_934037.1:n.487T>A
XR_934038.1:n.487T>A
XR_934039.1:n.487T>A
XM_011523918.2:c.-173T>A	XP_011522220.1:n.-173T>A
XM_017024714.2:c.-173T>A	XP_016880203.1:n.-173T>A
XM_017024715.2:c.-173T>A	XP_016880204.1:n.-173T>A
XM_024450780.1:c.-173T>A	XP_024306548.1:n.-173T>A
XM_024450781.1:c.-173T>A	XP_024306549.1:n.-173T>A
XM_024450782.1:c.-173T>A	XP_024306550.1:n.-173T>A
XR_934039.2:n.526T>A
NM_016239.4:c.-173T>A MANE Select	NP_057323.3:n.-173T>A