Canonical Allele Identifier: CA2636444214

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18143809-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18143809C>A , CM000679.2:g.18143809C>A	GRCh38
NC_000017.10:g.18047123C>A , CM000679.1:g.18047123C>A	GRCh37
NC_000017.9:g.17987848C>A	NCBI36
NG_011634.1:g.40104C>A
NG_011634.2:g.40104C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6046+13C>A MANE Select	ENSP00000495481.1:n.6046+13C>A
ENST00000205890.9:c.6046+13C>A	ENSP00000205890.5:n.6046+13C>A
ENST00000615845.4:c.6046+13C>A	ENSP00000481642.1:n.6046+13C>A
NM_016239.3:c.6046+13C>A	NP_057323.3:n.6046+13C>A
XM_011523917.1:c.5986+13C>A	XP_011522219.1:n.5986+13C>A
XM_011523918.1:c.5986+13C>A	XP_011522220.1:n.5986+13C>A
XM_011523919.1:c.5986+13C>A	XP_011522221.1:n.5986+13C>A
XM_011523921.1:c.6040+13C>A	XP_011522223.1:n.6040+13C>A
XR_934037.1:n.6645+13C>A
XR_934038.1:n.6645+13C>A
XM_011523918.2:c.5986+13C>A	XP_011522220.1:n.5986+13C>A
XM_017024714.2:c.5986+13C>A	XP_016880203.1:n.5986+13C>A
XM_017024715.2:c.6049+13C>A	XP_016880204.1:n.6049+13C>A
XM_024450780.1:c.5986+13C>A	XP_024306548.1:n.5986+13C>A
XM_024450781.1:c.5986+13C>A	XP_024306549.1:n.5986+13C>A
NM_016239.4:c.6046+13C>A MANE Select	NP_057323.3:n.6046+13C>A