Canonical Allele Identifier: CA726647298

Gene: MYO15A

Linked Data

• dbSNP Id: rs1338466953
• gnomAD v4: 17-18150374-G-A
• MyVariant Identifiers: chr17:g.18053688G>A (hg19) ; chr17:g.18150374G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150374G>A , CM000679.2:g.18150374G>A	GRCh38
NC_000017.10:g.18053688G>A , CM000679.1:g.18053688G>A	GRCh37
NC_000017.9:g.17994413G>A	NCBI36
NG_011634.1:g.46669G>A
NG_011634.2:g.46669G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647165.2:c.7213-55G>A MANE Select	ENSP00000495481.1:n.7213-55G>A
ENST00000205890.9:c.7213-55G>A	ENSP00000205890.5:n.7213-55G>A
ENST00000615845.4:c.7213-55G>A	ENSP00000481642.1:n.7213-55G>A
NM_016239.3:c.7213-55G>A	NP_057323.3:n.7213-55G>A
XM_011523917.1:c.6888-55G>A	XP_011522219.1:n.6888-55G>A
XM_011523921.1:c.7207-55G>A	XP_011522223.1:n.7207-55G>A
XR_934037.1:n.7547-55G>A
XR_934038.1:n.7499-55G>A
XR_934293.1:n.434+1229C>T
XR_934294.1:n.435-601C>T
XR_934295.1:n.253+1229C>T
XM_017024714.2:c.7153-55G>A	XP_016880203.1:n.7153-55G>A
XM_017024715.2:c.7216-55G>A	XP_016880204.1:n.7216-55G>A
XR_934293.2:n.377+1229C>T
XR_934294.2:n.378-601C>T
NM_016239.4:c.7213-55G>A MANE Select	NP_057323.3:n.7213-55G>A