Canonical Allele Identifier: CA1260140044
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71643929G= , CM000664.2:g.71643929G= GRCh38
NC_000002.11:g.71871059G= , CM000664.1:g.71871059G= GRCh37
NC_000002.10:g.71724567G= NCBI36
NG_008694.1:g.195307G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698057.1:c.1942-36G= ENSP00000513536.1:n.1942-36G=
ENST00000698058.1:c.1159-36G= ENSP00000513537.1:n.1159-36G=
ENST00000698059.1:c.1267-36G= ENSP00000513538.1:n.1267-36G=
ENST00000258104.8:c.4411-36G= MANE Plus Clinical ENSP00000258104.3:n.4411-36G=
ENST00000410020.8:c.4528-36G= MANE Select ENSP00000386881.3:n.4528-36G=
ENST00000258104.7:c.4411-36G= ENSP00000258104.3:n.4411-36G=
ENST00000394120.6:c.4414-36G= ENSP00000377678.2:n.4414-36G=
ENST00000409366.5:c.4477-36G= ENSP00000386512.1:n.4477-36G=
ENST00000409582.7:c.4525-36G= ENSP00000386547.3:n.4525-36G=
ENST00000409651.5:c.4507-36G= ENSP00000386683.1:n.4507-36G=
ENST00000409744.5:c.4435-36G= ENSP00000386285.1:n.4435-36G=
ENST00000409762.5:c.4462-36G= ENSP00000387137.1:n.4462-36G=
ENST00000410020.7:c.4528-36G= ENSP00000386881.3:n.4528-36G=
ENST00000410041.1:c.4465-36G= ENSP00000386617.1:n.4465-36G=
ENST00000413539.6:c.4504-36G= ENSP00000407046.2:n.4504-36G=
ENST00000429174.6:c.4474-36G= ENSP00000398305.2:n.4474-36G=
ENST00000468173.1:n.710-36G=
ENST00000479049.6:n.1296-36G=
NM_001130455.1:c.4414-36G= NP_001123927.1:n.4414-36G=
NM_001130976.1:c.4369-36G= NP_001124448.1:n.4369-36G=
NM_001130977.1:c.4432-36G= NP_001124449.1:n.4432-36G=
NM_001130978.1:c.4474-36G= NP_001124450.1:n.4474-36G=
NM_001130979.1:c.4504-36G= NP_001124451.1:n.4504-36G=
NM_001130980.1:c.4462-36G= NP_001124452.1:n.4462-36G=
NM_001130981.1:c.4525-36G= NP_001124453.1:n.4525-36G=
NM_001130982.1:c.4507-36G= NP_001124454.1:n.4507-36G=
NM_001130983.1:c.4477-36G= NP_001124455.1:n.4477-36G=
NM_001130984.1:c.4435-36G= NP_001124456.1:n.4435-36G=
NM_001130985.1:c.4465-36G= NP_001124457.1:n.4465-36G=
NM_001130986.1:c.4372-36G= NP_001124458.1:n.4372-36G=
NM_001130987.1:c.4528-36G= NP_001124459.1:n.4528-36G=
NM_003494.3:c.4411-36G= NP_003485.1:n.4411-36G=
XM_005264584.3:c.4570-36G= XP_005264641.1:n.4570-36G=
XM_005264585.3:c.4567-36G= XP_005264642.1:n.4567-36G=
XM_005264584.4:c.4570-36G= XP_005264641.1:n.4570-36G=
XM_005264585.5:c.4567-36G= XP_005264642.1:n.4567-36G=
XR_001738969.1:n.4728-36G=
NM_001130987.2:c.4528-36G= MANE Select NP_001124459.1:n.4528-36G=
NM_001130455.2:c.4414-36G= NP_001123927.1:n.4414-36G=
NM_001130976.2:c.4369-36G= NP_001124448.1:n.4369-36G=
NM_001130977.2:c.4432-36G= NP_001124449.1:n.4432-36G=
NM_001130978.2:c.4474-36G= NP_001124450.1:n.4474-36G=
NM_001130979.2:c.4504-36G= NP_001124451.1:n.4504-36G=
NM_001130980.2:c.4462-36G= NP_001124452.1:n.4462-36G=
NM_001130981.2:c.4525-36G= NP_001124453.1:n.4525-36G=
NM_001130982.2:c.4507-36G= NP_001124454.1:n.4507-36G=
NM_001130983.2:c.4477-36G= NP_001124455.1:n.4477-36G=
NM_001130984.2:c.4435-36G= NP_001124456.1:n.4435-36G=
NM_001130985.2:c.4465-36G= NP_001124457.1:n.4465-36G=
NM_001130986.2:c.4372-36G= NP_001124458.1:n.4372-36G=
NM_003494.4:c.4411-36G= MANE Plus Clinical NP_003485.1:n.4411-36G=