Canonical Allele Identifier: CA2586969510

Gene: DYSF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71643968_71643990del , CM000664.2:g.71643968_71643990del	GRCh38
NC_000002.11:g.71871098_71871120del , CM000664.1:g.71871098_71871120del	GRCh37
NC_000002.10:g.71724606_71724628del	NCBI36
NG_008694.1:g.195346_195368del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.1945_1967del
ENST00000698058.1:c.1162_1184del
ENST00000698059.1:c.1270_1292del
ENST00000258104.8:c.4414_4436del
ENST00000410020.8:c.4531_4553del
ENST00000258104.7:c.4414_4436del
ENST00000394120.6:c.4417_4439del
ENST00000409366.5:c.4480_4502del
ENST00000409582.7:c.4528_4550del
ENST00000409651.5:c.4510_4532del
ENST00000409744.5:c.4438_4460del
ENST00000409762.5:c.4465_4487del
ENST00000410020.7:c.4531_4553del
ENST00000410041.1:c.4468_4490del
ENST00000413539.6:c.4507_4529del
ENST00000429174.6:c.4477_4499del
ENST00000468173.1:n.713_735del
ENST00000479049.6:n.1299_1321del
NM_001130455.1:c.4417_4439del
NM_001130976.1:c.4372_4394del
NM_001130977.1:c.4435_4457del
NM_001130978.1:c.4477_4499del
NM_001130979.1:c.4507_4529del
NM_001130980.1:c.4465_4487del
NM_001130981.1:c.4528_4550del
NM_001130982.1:c.4510_4532del
NM_001130983.1:c.4480_4502del
NM_001130984.1:c.4438_4460del
NM_001130985.1:c.4468_4490del
NM_001130986.1:c.4375_4397del
NM_001130987.1:c.4531_4553del
NM_003494.3:c.4414_4436del
XM_005264584.3:c.4573_4595del
XM_005264585.3:c.4570_4592del
XM_005264584.4:c.4573_4595del
XM_005264585.5:c.4570_4592del
XR_001738969.1:n.4731_4753del
NM_001130987.2:c.4531_4553del
NM_001130455.2:c.4417_4439del
NM_001130976.2:c.4372_4394del
NM_001130977.2:c.4435_4457del
NM_001130978.2:c.4477_4499del
NM_001130979.2:c.4507_4529del
NM_001130980.2:c.4465_4487del
NM_001130981.2:c.4528_4550del
NM_001130982.2:c.4510_4532del
NM_001130983.2:c.4480_4502del
NM_001130984.2:c.4438_4460del
NM_001130985.2:c.4468_4490del
NM_001130986.2:c.4375_4397del
NM_003494.4:c.4414_4436del