Canonical Allele Identifier: CA498427955

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18119913-C-G
• MyVariant Identifiers: chr17:g.18023227C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18119913C>G , CM000679.2:g.18119913C>G	GRCh38
NC_000017.10:g.18023227C>G , CM000679.1:g.18023227C>G	GRCh37
NC_000017.9:g.17963952C>G	NCBI36
NG_011634.1:g.16208C>G
NG_011634.2:g.16208C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647165.2:c.1113C>G MANE Select	ENSP00000495481.1:p.Pro371=
ENST00000205890.9:c.1113C>G	ENSP00000205890.5:p.Pro371=
ENST00000583079.1:n.746C>G
ENST00000615845.4:c.1113C>G	ENSP00000481642.1:p.Pro371=
NM_016239.3:c.1113C>G	NP_057323.3:p.Pro371=
XM_011523917.1:c.1113C>G	XP_011522219.1:p.Pro371=
XM_011523918.1:c.1113C>G	XP_011522220.1:p.Pro371=
XM_011523919.1:c.1113C>G	XP_011522221.1:p.Pro371=
XM_011523920.1:c.1113C>G	XP_011522222.1:p.Pro371=
XM_011523921.1:c.1113C>G	XP_011522223.1:p.Pro371=
XR_934037.1:n.1772C>G
XR_934038.1:n.1772C>G
XR_934039.1:n.1772C>G
XM_011523918.2:c.1113C>G	XP_011522220.1:p.Pro371=
XM_017024714.2:c.1113C>G	XP_016880203.1:p.Pro371=
XM_017024715.2:c.1113C>G	XP_016880204.1:p.Pro371=
XM_024450780.1:c.1113C>G	XP_024306548.1:p.Pro371=
XM_024450781.1:c.1113C>G	XP_024306549.1:p.Pro371=
XM_024450782.1:c.1113C>G	XP_024306550.1:p.Pro371=
XR_934039.2:n.1811C>G
NM_016239.4:c.1113C>G MANE Select	NP_057323.3:p.Pro371=