Canonical Allele Identifier: CA1260156848
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71679110A= , CM000664.2:g.71679110A= GRCh38
NC_000002.11:g.71906240A= , CM000664.1:g.71906240A= GRCh37
NC_000002.10:g.71759748A= NCBI36
NG_008694.1:g.230488A=

Transcript Alleles

HGVS Amino-acid change
ENST00000698057.1:c.3352A= ENSP00000513536.1:p.Lys1118=
ENST00000698058.1:c.2569A= ENSP00000513537.1:p.Lys857=
ENST00000698059.1:c.2677A= ENSP00000513538.1:p.Lys893=
ENST00000258104.8:c.5821A= MANE Plus Clinical ENSP00000258104.3:p.Lys1941=
ENST00000410020.8:c.5938A= MANE Select ENSP00000386881.3:p.Lys1980=
ENST00000258104.7:c.5821A= ENSP00000258104.3:p.Lys1941=
ENST00000394120.6:c.5824A= ENSP00000377678.2:p.Lys1942=
ENST00000409366.5:c.5887A= ENSP00000386512.1:p.Lys1963=
ENST00000409582.7:c.5935A= ENSP00000386547.3:p.Lys1979=
ENST00000409651.5:c.5917A= ENSP00000386683.1:p.Lys1973=
ENST00000409744.5:c.5845A= ENSP00000386285.1:p.Lys1949=
ENST00000409762.5:c.5872A= ENSP00000387137.1:p.Lys1958=
ENST00000410020.7:c.5938A= ENSP00000386881.3:p.Lys1980=
ENST00000410041.1:c.5875A= ENSP00000386617.1:p.Lys1959=
ENST00000413539.6:c.5914A= ENSP00000407046.2:p.Lys1972=
ENST00000429174.6:c.5884A= ENSP00000398305.2:p.Lys1962=
ENST00000479049.6:n.2706A=
NM_001130455.1:c.5824A= NP_001123927.1:p.Lys1942=
NM_001130976.1:c.5779A= NP_001124448.1:p.Lys1927=
NM_001130977.1:c.5842A= NP_001124449.1:p.Lys1948=
NM_001130978.1:c.5884A= NP_001124450.1:p.Lys1962=
NM_001130979.1:c.5914A= NP_001124451.1:p.Lys1972=
NM_001130980.1:c.5872A= NP_001124452.1:p.Lys1958=
NM_001130981.1:c.5935A= NP_001124453.1:p.Lys1979=
NM_001130982.1:c.5917A= NP_001124454.1:p.Lys1973=
NM_001130983.1:c.5887A= NP_001124455.1:p.Lys1963=
NM_001130984.1:c.5845A= NP_001124456.1:p.Lys1949=
NM_001130985.1:c.5875A= NP_001124457.1:p.Lys1959=
NM_001130986.1:c.5782A= NP_001124458.1:p.Lys1928=
NM_001130987.1:c.5938A= NP_001124459.1:p.Lys1980=
NM_003494.3:c.5821A= NP_003485.1:p.Lys1941=
XM_005264584.3:c.5980A= XP_005264641.1:p.Lys1994=
XM_005264585.3:c.5977A= XP_005264642.1:p.Lys1993=
XM_005264584.4:c.5980A= XP_005264641.1:p.Lys1994=
XM_005264585.5:c.5977A= XP_005264642.1:p.Lys1993=
NM_001130987.2:c.5938A= MANE Select NP_001124459.1:p.Lys1980=
NM_001130455.2:c.5824A= NP_001123927.1:p.Lys1942=
NM_001130976.2:c.5779A= NP_001124448.1:p.Lys1927=
NM_001130977.2:c.5842A= NP_001124449.1:p.Lys1948=
NM_001130978.2:c.5884A= NP_001124450.1:p.Lys1962=
NM_001130979.2:c.5914A= NP_001124451.1:p.Lys1972=
NM_001130980.2:c.5872A= NP_001124452.1:p.Lys1958=
NM_001130981.2:c.5935A= NP_001124453.1:p.Lys1979=
NM_001130982.2:c.5917A= NP_001124454.1:p.Lys1973=
NM_001130983.2:c.5887A= NP_001124455.1:p.Lys1963=
NM_001130984.2:c.5845A= NP_001124456.1:p.Lys1949=
NM_001130985.2:c.5875A= NP_001124457.1:p.Lys1959=
NM_001130986.2:c.5782A= NP_001124458.1:p.Lys1928=
NM_003494.4:c.5821A= MANE Plus Clinical NP_003485.1:p.Lys1941=