Canonical Allele Identifier: CA2576190681

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150352A>G , CM000679.2:g.18150352A>G	GRCh38
NC_000017.10:g.18053666A>G , CM000679.1:g.18053666A>G	GRCh37
NC_000017.9:g.17994391A>G	NCBI36
NG_011634.1:g.46647A>G
NG_011634.2:g.46647A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7213-77A>G MANE Select	ENSP00000495481.1:n.7213-77A>G
ENST00000205890.9:c.7213-77A>G	ENSP00000205890.5:n.7213-77A>G
ENST00000615845.4:c.7213-77A>G	ENSP00000481642.1:n.7213-77A>G
NM_016239.3:c.7213-77A>G	NP_057323.3:n.7213-77A>G
XM_011523917.1:c.6888-77A>G	XP_011522219.1:n.6888-77A>G
XM_011523921.1:c.7207-77A>G	XP_011522223.1:n.7207-77A>G
XR_934037.1:n.7547-77A>G
XR_934038.1:n.7499-77A>G
XR_934293.1:n.434+1251T>C
XR_934294.1:n.435-579T>C
XR_934295.1:n.253+1251T>C
XM_017024714.2:c.7153-77A>G	XP_016880203.1:n.7153-77A>G
XM_017024715.2:c.7216-77A>G	XP_016880204.1:n.7216-77A>G
XR_934293.2:n.377+1251T>C
XR_934294.2:n.378-579T>C
NM_016239.4:c.7213-77A>G MANE Select	NP_057323.3:n.7213-77A>G