Canonical Allele Identifier: CA1260152222
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71669191G= , CM000664.2:g.71669191G= GRCh38
NC_000002.11:g.71896321G= , CM000664.1:g.71896321G= GRCh37
NC_000002.10:g.71749829G= NCBI36
NG_008694.1:g.220569G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698057.1:c.3040G= ENSP00000513536.1:p.Asp1014=
ENST00000698058.1:c.2257G= ENSP00000513537.1:p.Asp753=
ENST00000698059.1:c.2365G= ENSP00000513538.1:p.Asp789=
ENST00000258104.8:c.5509G= MANE Plus Clinical ENSP00000258104.3:p.Asp1837=
ENST00000410020.8:c.5626G= MANE Select ENSP00000386881.3:p.Asp1876=
ENST00000258104.7:c.5509G= ENSP00000258104.3:p.Asp1837=
ENST00000394120.6:c.5512G= ENSP00000377678.2:p.Asp1838=
ENST00000409366.5:c.5575G= ENSP00000386512.1:p.Asp1859=
ENST00000409582.7:c.5623G= ENSP00000386547.3:p.Asp1875=
ENST00000409651.5:c.5605G= ENSP00000386683.1:p.Asp1869=
ENST00000409744.5:c.5533G= ENSP00000386285.1:p.Asp1845=
ENST00000409762.5:c.5560G= ENSP00000387137.1:p.Asp1854=
ENST00000410020.7:c.5626G= ENSP00000386881.3:p.Asp1876=
ENST00000410041.1:c.5563G= ENSP00000386617.1:p.Asp1855=
ENST00000413539.6:c.5602G= ENSP00000407046.2:p.Asp1868=
ENST00000429174.6:c.5572G= ENSP00000398305.2:p.Asp1858=
ENST00000479049.6:n.2394G=
NM_001130455.1:c.5512G= NP_001123927.1:p.Asp1838=
NM_001130976.1:c.5467G= NP_001124448.1:p.Asp1823=
NM_001130977.1:c.5530G= NP_001124449.1:p.Asp1844=
NM_001130978.1:c.5572G= NP_001124450.1:p.Asp1858=
NM_001130979.1:c.5602G= NP_001124451.1:p.Asp1868=
NM_001130980.1:c.5560G= NP_001124452.1:p.Asp1854=
NM_001130981.1:c.5623G= NP_001124453.1:p.Asp1875=
NM_001130982.1:c.5605G= NP_001124454.1:p.Asp1869=
NM_001130983.1:c.5575G= NP_001124455.1:p.Asp1859=
NM_001130984.1:c.5533G= NP_001124456.1:p.Asp1845=
NM_001130985.1:c.5563G= NP_001124457.1:p.Asp1855=
NM_001130986.1:c.5470G= NP_001124458.1:p.Asp1824=
NM_001130987.1:c.5626G= NP_001124459.1:p.Asp1876=
NM_003494.3:c.5509G= NP_003485.1:p.Asp1837=
XM_005264584.3:c.5668G= XP_005264641.1:p.Asp1890=
XM_005264585.3:c.5665G= XP_005264642.1:p.Asp1889=
XM_005264584.4:c.5668G= XP_005264641.1:p.Asp1890=
XM_005264585.5:c.5665G= XP_005264642.1:p.Asp1889=
NM_001130987.2:c.5626G= MANE Select NP_001124459.1:p.Asp1876=
NM_001130455.2:c.5512G= NP_001123927.1:p.Asp1838=
NM_001130976.2:c.5467G= NP_001124448.1:p.Asp1823=
NM_001130977.2:c.5530G= NP_001124449.1:p.Asp1844=
NM_001130978.2:c.5572G= NP_001124450.1:p.Asp1858=
NM_001130979.2:c.5602G= NP_001124451.1:p.Asp1868=
NM_001130980.2:c.5560G= NP_001124452.1:p.Asp1854=
NM_001130981.2:c.5623G= NP_001124453.1:p.Asp1875=
NM_001130982.2:c.5605G= NP_001124454.1:p.Asp1869=
NM_001130983.2:c.5575G= NP_001124455.1:p.Asp1859=
NM_001130984.2:c.5533G= NP_001124456.1:p.Asp1845=
NM_001130985.2:c.5563G= NP_001124457.1:p.Asp1855=
NM_001130986.2:c.5470G= NP_001124458.1:p.Asp1824=
NM_003494.4:c.5509G= MANE Plus Clinical NP_003485.1:p.Asp1837=