Canonical Allele Identifier: CA2573153136

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18172234_18172248del , CM000679.2:g.18172234_18172248del	GRCh38
NC_000017.10:g.18075548_18075562del , CM000679.1:g.18075548_18075562del	GRCh37
NC_000017.9:g.18016273_18016287del	NCBI36
NG_011634.1:g.68529_68543del
NG_011634.2:g.68529_68543del

Transcript Alleles

HGVS	Amino-acid Change
NM_016239.4:c.10294_10308del MANE Select	NP_057323.3:p.Pro3432_Ala3436del
ENST00000647165.2:c.10294_10308del MANE Select	ENSP00000495481.1:p.Pro3432_Ala3436del
NM_016239.3:c.10294_10308del	NP_057323.3:p.Pro3432_Ala3436del
ENST00000205890.9:c.10294_10308del	ENSP00000205890.5:p.Pro3432_Ala3436del
ENST00000418233.7:c.2086_2100del	ENSP00000408800.3:p.Pro696_Ala700del
ENST00000433411.7:n.1694_1708del
ENST00000445289.6:n.1063_1077del
ENST00000578575.1:c.836_850del
ENST00000579848.6:c.714_728del	ENSP00000465910.1:p.Leu239_Pro243del
ENST00000615845.4:c.10294_10308del	ENSP00000481642.1:p.Pro3432_Ala3436del
ENST00000642418.1:n.2648_2662del
ENST00000643693.1:n.2236_2250del
ENST00000644795.1:c.2036_2050del	ENSP00000495720.1:p.Pro679_Cys683del
ENST00000646782.1:n.2978_2992del
ENST00000651214.1:n.2725_2739del
XM_011523921.1:c.10288_10302del	XP_011522223.1:p.Pro3430_Ala3434del
XM_017024714.2:c.10234_10248del	XP_016880203.1:p.Pro3412_Ala3416del
XM_017024715.2:c.10297_10311del	XP_016880204.1:p.Pro3433_Ala3437del