Canonical Allele Identifier: CA2636437661

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18149438-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18149438A>T , CM000679.2:g.18149438A>T	GRCh38
NC_000017.10:g.18052752A>T , CM000679.1:g.18052752A>T	GRCh37
NC_000017.9:g.17993477A>T	NCBI36
NG_011634.1:g.45733A>T
NG_011634.2:g.45733A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7118-48A>T MANE Select	ENSP00000495481.1:n.7118-48A>T
ENST00000205890.9:c.7118-48A>T	ENSP00000205890.5:n.7118-48A>T
ENST00000578999.1:n.691A>T
ENST00000615845.4:c.7118-48A>T	ENSP00000481642.1:n.7118-48A>T
NM_016239.3:c.7118-48A>T	NP_057323.3:n.7118-48A>T
XM_011523917.1:c.6793-48A>T	XP_011522219.1:n.6793-48A>T
XM_011523921.1:c.7112-48A>T	XP_011522223.1:n.7112-48A>T
XR_934037.1:n.7452-48A>T
XR_934038.1:n.7404-48A>T
XR_934293.1:n.435-1832T>A
XR_934295.1:n.254-1832T>A
XM_017024714.2:c.7058-48A>T	XP_016880203.1:n.7058-48A>T
XM_017024715.2:c.7121-48A>T	XP_016880204.1:n.7121-48A>T
XR_934293.2:n.378-1832T>A
NM_016239.4:c.7118-48A>T MANE Select	NP_057323.3:n.7118-48A>T