Canonical Allele Identifier: CA398605113

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18143584T>G , CM000679.2:g.18143584T>G	GRCh38
NC_000017.10:g.18046898T>G , CM000679.1:g.18046898T>G	GRCh37
NC_000017.9:g.17987623T>G	NCBI36
NG_011634.1:g.39879T>G
NG_011634.2:g.39879T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.5929T>G MANE Select	ENSP00000495481.1:p.Cys1977Gly
ENST00000205890.9:c.5929T>G	ENSP00000205890.5:p.Cys1977Gly
ENST00000615845.4:c.5929T>G	ENSP00000481642.1:p.Cys1977Gly
NM_016239.3:c.5929T>G	NP_057323.3:p.Cys1977Gly
XM_011523917.1:c.5905-131T>G	XP_011522219.1:n.5905-131T>G
XM_011523918.1:c.5905-131T>G	XP_011522220.1:n.5905-131T>G
XM_011523919.1:c.5905-131T>G	XP_011522221.1:n.5905-131T>G
XM_011523920.1:c.*36T>G	XP_011522222.1:n.*36T>G
XM_011523921.1:c.5923T>G	XP_011522223.1:p.Cys1975Gly
XR_934037.1:n.6564-131T>G
XR_934038.1:n.6564-131T>G
XR_934039.1:n.6821T>G
XM_011523918.2:c.5905-131T>G	XP_011522220.1:n.5905-131T>G
XM_017024714.2:c.5905-131T>G	XP_016880203.1:n.5905-131T>G
XM_017024715.2:c.5932T>G	XP_016880204.1:p.Cys1978Gly
XM_024450780.1:c.5905-131T>G	XP_024306548.1:n.5905-131T>G
XM_024450781.1:c.5905-131T>G	XP_024306549.1:n.5905-131T>G
XM_024450782.1:c.*36T>G	XP_024306550.1:n.*36T>G
XR_934039.2:n.6860T>G
NM_016239.4:c.5929T>G MANE Select	NP_057323.3:p.Cys1977Gly