Canonical Allele Identifier: CA398610310

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18148108C>G , CM000679.2:g.18148108C>G	GRCh38
NC_000017.10:g.18051422C>G , CM000679.1:g.18051422C>G	GRCh37
NC_000017.9:g.17992147C>G	NCBI36
NG_011634.1:g.44403C>G
NG_011634.2:g.44403C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6589C>G MANE Select	ENSP00000495481.1:p.Gln2197Glu
ENST00000205890.9:c.6589C>G	ENSP00000205890.5:p.Gln2197Glu
ENST00000578999.1:n.174C>G
ENST00000615845.4:c.6589C>G	ENSP00000481642.1:p.Gln2197Glu
NM_016239.3:c.6589C>G	NP_057323.3:p.Gln2197Glu
XM_011523917.1:c.6529C>G	XP_011522219.1:p.Gln2177Glu
XM_011523918.1:c.*68C>G	XP_011522220.1:n.*68C>G
XM_011523921.1:c.6583C>G	XP_011522223.1:p.Gln2195Glu
XR_934037.1:n.7188C>G
XR_934038.1:n.7188C>G
XR_934293.1:n.435-502G>C
XR_934295.1:n.254-502G>C
XM_011523918.2:c.*68C>G	XP_011522220.1:n.*68C>G
XM_017024714.2:c.6529C>G	XP_016880203.1:p.Gln2177Glu
XM_017024715.2:c.6592C>G	XP_016880204.1:p.Gln2198Glu
XM_024450781.1:c.*68C>G	XP_024306549.1:n.*68C>G
XR_934293.2:n.378-502G>C
NM_016239.4:c.6589C>G MANE Select	NP_057323.3:p.Gln2197Glu