Canonical Allele Identifier: CA2636439802

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18150363-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150363C>G , CM000679.2:g.18150363C>G	GRCh38
NC_000017.10:g.18053677C>G , CM000679.1:g.18053677C>G	GRCh37
NC_000017.9:g.17994402C>G	NCBI36
NG_011634.1:g.46658C>G
NG_011634.2:g.46658C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7213-66C>G MANE Select	ENSP00000495481.1:n.7213-66C>G
ENST00000205890.9:c.7213-66C>G	ENSP00000205890.5:n.7213-66C>G
ENST00000615845.4:c.7213-66C>G	ENSP00000481642.1:n.7213-66C>G
NM_016239.3:c.7213-66C>G	NP_057323.3:n.7213-66C>G
XM_011523917.1:c.6888-66C>G	XP_011522219.1:n.6888-66C>G
XM_011523921.1:c.7207-66C>G	XP_011522223.1:n.7207-66C>G
XR_934037.1:n.7547-66C>G
XR_934038.1:n.7499-66C>G
XR_934293.1:n.434+1240G>C
XR_934294.1:n.435-590G>C
XR_934295.1:n.253+1240G>C
XM_017024714.2:c.7153-66C>G	XP_016880203.1:n.7153-66C>G
XM_017024715.2:c.7216-66C>G	XP_016880204.1:n.7216-66C>G
XR_934293.2:n.377+1240G>C
XR_934294.2:n.378-590G>C
NM_016239.4:c.7213-66C>G MANE Select	NP_057323.3:n.7213-66C>G