Canonical Allele Identifier: CA2695200833
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 2674958
ClinVar RCV Id: RCV003467862

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71669207_71669219del , CM000664.2:g.71669207_71669219del GRCh38
NC_000002.11:g.71896337_71896349del , CM000664.1:g.71896337_71896349del GRCh37
NC_000002.10:g.71749845_71749857del NCBI36
NG_008694.1:g.220585_220597del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698057.1:c.3056_3056+12del
ENST00000698058.1:c.2273_2273+12del
ENST00000698059.1:c.2381_2381+12del
ENST00000258104.8:c.5525_5525+12del
ENST00000410020.8:c.5642_5642+12del
ENST00000258104.7:c.5525_5525+12del
ENST00000394120.6:c.5528_5528+12del
ENST00000409366.5:c.5591_5591+12del
ENST00000409582.7:c.5639_5639+12del
ENST00000409651.5:c.5621_5621+12del
ENST00000409744.5:c.5549_5549+12del
ENST00000409762.5:c.5576_5576+12del
ENST00000410020.7:c.5642_5642+12del
ENST00000410041.1:c.5579_5579+12del
ENST00000413539.6:c.5618_5618+12del
ENST00000429174.6:c.5588_5588+12del
ENST00000479049.6:n.2410_2410+12del
NM_001130455.1:c.5528_5528+12del
NM_001130976.1:c.5483_5483+12del
NM_001130977.1:c.5546_5546+12del
NM_001130978.1:c.5588_5588+12del
NM_001130979.1:c.5618_5618+12del
NM_001130980.1:c.5576_5576+12del
NM_001130981.1:c.5639_5639+12del
NM_001130982.1:c.5621_5621+12del
NM_001130983.1:c.5591_5591+12del
NM_001130984.1:c.5549_5549+12del
NM_001130985.1:c.5579_5579+12del
NM_001130986.1:c.5486_5486+12del
NM_001130987.1:c.5642_5642+12del
NM_003494.3:c.5525_5525+12del
XM_005264584.3:c.5684_5684+12del
XM_005264585.3:c.5681_5681+12del
XM_005264584.4:c.5684_5684+12del
XM_005264585.5:c.5681_5681+12del
NM_001130987.2:c.5642_5642+12del
NM_001130455.2:c.5528_5528+12del
NM_001130976.2:c.5483_5483+12del
NM_001130977.2:c.5546_5546+12del
NM_001130978.2:c.5588_5588+12del
NM_001130979.2:c.5618_5618+12del
NM_001130980.2:c.5576_5576+12del
NM_001130981.2:c.5639_5639+12del
NM_001130982.2:c.5621_5621+12del
NM_001130983.2:c.5591_5591+12del
NM_001130984.2:c.5549_5549+12del
NM_001130985.2:c.5579_5579+12del
NM_001130986.2:c.5486_5486+12del
NM_003494.4:c.5525_5525+12del