Canonical Allele Identifier: CA1260095697
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71553143C= , CM000664.2:g.71553143C= GRCh38
NC_000002.11:g.71780273C= , CM000664.1:g.71780273C= GRCh37
NC_000002.10:g.71633781C= NCBI36
NG_008694.1:g.104521C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258104.8:c.1885C= MANE Plus Clinical ENSP00000258104.3:p.Leu629=
ENST00000410020.8:c.1939C= MANE Select ENSP00000386881.3:p.Leu647=
ENST00000258104.7:c.1885C= ENSP00000258104.3:p.Leu629=
ENST00000394120.6:c.1888C= ENSP00000377678.2:p.Leu630=
ENST00000409366.5:c.1888C= ENSP00000386512.1:p.Leu630=
ENST00000409582.7:c.1936C= ENSP00000386547.3:p.Leu646=
ENST00000409651.5:c.1981C= ENSP00000386683.1:p.Leu661=
ENST00000409744.5:c.1846C= ENSP00000386285.1:p.Leu616=
ENST00000409762.5:c.1936C= ENSP00000387137.1:p.Leu646=
ENST00000410020.7:c.1939C= ENSP00000386881.3:p.Leu647=
ENST00000410041.1:c.1939C= ENSP00000386617.1:p.Leu647=
ENST00000413539.6:c.1978C= ENSP00000407046.2:p.Leu660=
ENST00000429174.6:c.1885C= ENSP00000398305.2:p.Leu629=
NM_001130455.1:c.1888C= NP_001123927.1:p.Leu630=
NM_001130976.1:c.1843C= NP_001124448.1:p.Leu615=
NM_001130977.1:c.1843C= NP_001124449.1:p.Leu615=
NM_001130978.1:c.1885C= NP_001124450.1:p.Leu629=
NM_001130979.1:c.1978C= NP_001124451.1:p.Leu660=
NM_001130980.1:c.1936C= NP_001124452.1:p.Leu646=
NM_001130981.1:c.1936C= NP_001124453.1:p.Leu646=
NM_001130982.1:c.1981C= NP_001124454.1:p.Leu661=
NM_001130983.1:c.1888C= NP_001124455.1:p.Leu630=
NM_001130984.1:c.1846C= NP_001124456.1:p.Leu616=
NM_001130985.1:c.1939C= NP_001124457.1:p.Leu647=
NM_001130986.1:c.1846C= NP_001124458.1:p.Leu616=
NM_001130987.1:c.1939C= NP_001124459.1:p.Leu647=
NM_003494.3:c.1885C= NP_003485.1:p.Leu629=
XM_005264584.3:c.1981C= XP_005264641.1:p.Leu661=
XM_005264585.3:c.1978C= XP_005264642.1:p.Leu660=
XM_005264584.4:c.1981C= XP_005264641.1:p.Leu661=
XM_005264585.5:c.1978C= XP_005264642.1:p.Leu660=
XR_001738969.1:n.2139C=
NM_001130987.2:c.1939C= MANE Select NP_001124459.1:p.Leu647=
NM_001130455.2:c.1888C= NP_001123927.1:p.Leu630=
NM_001130976.2:c.1843C= NP_001124448.1:p.Leu615=
NM_001130977.2:c.1843C= NP_001124449.1:p.Leu615=
NM_001130978.2:c.1885C= NP_001124450.1:p.Leu629=
NM_001130979.2:c.1978C= NP_001124451.1:p.Leu660=
NM_001130980.2:c.1936C= NP_001124452.1:p.Leu646=
NM_001130981.2:c.1936C= NP_001124453.1:p.Leu646=
NM_001130982.2:c.1981C= NP_001124454.1:p.Leu661=
NM_001130983.2:c.1888C= NP_001124455.1:p.Leu630=
NM_001130984.2:c.1846C= NP_001124456.1:p.Leu616=
NM_001130985.2:c.1939C= NP_001124457.1:p.Leu647=
NM_001130986.2:c.1846C= NP_001124458.1:p.Leu616=
NM_003494.4:c.1885C= MANE Plus Clinical NP_003485.1:p.Leu629=