Canonical Allele Identifier: CA16607541

Gene: MYO15A

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18166449G>A , CM000679.2:g.18166449G>A	GRCh38
NC_000017.10:g.18069763G>A , CM000679.1:g.18069763G>A	GRCh37
NC_000017.9:g.18010488G>A	NCBI36
NG_011634.1:g.62744G>A
NG_011634.2:g.62744G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.2140G>A
ENST00000643693.1:n.1678G>A
ENST00000644795.1:c.1668G>A	ENSP00000495720.1:p.Trp556Ter
ENST00000646782.1:n.2610G>A
ENST00000647165.2:c.9876G>A MANE Select	ENSP00000495481.1:p.Trp3292Ter
ENST00000651214.1:n.2307G>A
ENST00000205890.9:c.9876G>A	ENSP00000205890.5:p.Trp3292Ter
ENST00000418233.7:c.1668G>A	ENSP00000408800.3:p.Trp556Ter
ENST00000433411.7:n.1326G>A
ENST00000445289.6:n.718-1141G>A
ENST00000578575.1:c.351-1141G>A
ENST00000579848.6:c.502+2611G>A	ENSP00000465910.1:n.502+2611G>A
ENST00000615845.4:c.9876G>A	ENSP00000481642.1:p.Trp3292Ter
NM_016239.3:c.9876G>A	NP_057323.3:p.Trp3292Ter
XM_011523921.1:c.9870G>A	XP_011522223.1:p.Trp3290Ter
XM_017024714.2:c.9816G>A	XP_016880203.1:p.Trp3272Ter
XM_017024715.2:c.9879G>A	XP_016880204.1:p.Trp3293Ter
NM_016239.4:c.9876G>A MANE Select	NP_057323.3:p.Trp3292Ter