Canonical Allele Identifier: CA915942535
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 655612
ClinVar RCV Id: RCV000811827

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71566455_71570716del , CM000664.2:g.71566455_71570716del GRCh38
NC_000002.11:g.71793585_71797846del , CM000664.1:g.71793585_71797846del GRCh37
NC_000002.10:g.71647093_71651354del NCBI36
NG_008694.1:g.117833_122094del

Transcript Alleles

HGVS Amino-acid change
ENST00000258104.8:c.2512-1496_3149del
ENST00000410020.8:c.2566-1496_3203del
ENST00000258104.7:c.2512-1496_3149del
ENST00000394120.6:c.2515-1496_3152del
ENST00000409366.5:c.2515-1496_3152del
ENST00000409582.7:c.2563-1496_3200del
ENST00000409651.5:c.2608-1496_3245del
ENST00000409744.5:c.2473-1496_3110del
ENST00000409762.5:c.2563-1496_3200del
ENST00000410020.7:c.2566-1496_3203del
ENST00000410041.1:c.2566-1496_3203del
ENST00000413539.6:c.2605-1496_3242del
ENST00000429174.6:c.2512-1496_3149del
NM_001130455.1:c.2515-1496_3152del
NM_001130976.1:c.2470-1496_3107del
NM_001130977.1:c.2470-1496_3107del
NM_001130978.1:c.2512-1496_3149del
NM_001130979.1:c.2605-1496_3242del
NM_001130980.1:c.2563-1496_3200del
NM_001130981.1:c.2563-1496_3200del
NM_001130982.1:c.2608-1496_3245del
NM_001130983.1:c.2515-1496_3152del
NM_001130984.1:c.2473-1496_3110del
NM_001130985.1:c.2566-1496_3203del
NM_001130986.1:c.2473-1496_3110del
NM_001130987.1:c.2566-1496_3203del
NM_003494.3:c.2512-1496_3149del
XM_005264584.3:c.2608-1496_3245del
XM_005264585.3:c.2605-1496_3242del
XM_005264584.4:c.2608-1496_3245del
XM_005264585.5:c.2605-1496_3242del
XR_001738969.1:n.2766-1496_3403del
NM_001130987.2:c.2566-1496_3203del
NM_001130455.2:c.2515-1496_3152del
NM_001130976.2:c.2470-1496_3107del
NM_001130977.2:c.2470-1496_3107del
NM_001130978.2:c.2512-1496_3149del
NM_001130979.2:c.2605-1496_3242del
NM_001130980.2:c.2563-1496_3200del
NM_001130981.2:c.2563-1496_3200del
NM_001130982.2:c.2608-1496_3245del
NM_001130983.2:c.2515-1496_3152del
NM_001130984.2:c.2473-1496_3110del
NM_001130985.2:c.2566-1496_3203del
NM_001130986.2:c.2473-1496_3110del
NM_003494.4:c.2512-1496_3149del