Canonical Allele Identifier: CA1260099016
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71561966_71561969delinsTTTC , CM000664.2:g.71561966_71561969delinsTTTC GRCh38
NC_000002.11:g.71789096_71789099delinsTTTC , CM000664.1:g.71789096_71789099delinsTTTC GRCh37
NC_000002.10:g.71642604_71642607delinsTTTC NCBI36
NG_008694.1:g.113344_113347delinsTTTC

Transcript Alleles

HGVS Amino-acid change
ENST00000258104.8:c.2355+22_2355+25delinsTTTC MANE Plus Clinical ENSP00000258104.3:n.2355+22_2355+25delins...
ENST00000410020.8:c.2409+22_2409+25delinsTTTC MANE Select ENSP00000386881.3:n.2409+22_2409+25delins...
ENST00000258104.7:c.2355+22_2355+25delinsTTTC ENSP00000258104.3:n.2355+22_2355+25delins...
ENST00000394120.6:c.2358+22_2358+25delinsTTTC ENSP00000377678.2:n.2358+22_2358+25delins...
ENST00000409366.5:c.2358+22_2358+25delinsTTTC ENSP00000386512.1:n.2358+22_2358+25delins...
ENST00000409582.7:c.2406+22_2406+25delinsTTTC ENSP00000386547.3:n.2406+22_2406+25delins...
ENST00000409651.5:c.2451+22_2451+25delinsTTTC ENSP00000386683.1:n.2451+22_2451+25delins...
ENST00000409744.5:c.2316+22_2316+25delinsTTTC ENSP00000386285.1:n.2316+22_2316+25delins...
ENST00000409762.5:c.2406+22_2406+25delinsTTTC ENSP00000387137.1:n.2406+22_2406+25delins...
ENST00000410020.7:c.2409+22_2409+25delinsTTTC ENSP00000386881.3:n.2409+22_2409+25delins...
ENST00000410041.1:c.2409+22_2409+25delinsTTTC ENSP00000386617.1:n.2409+22_2409+25delins...
ENST00000413539.6:c.2448+22_2448+25delinsTTTC ENSP00000407046.2:n.2448+22_2448+25delins...
ENST00000429174.6:c.2355+22_2355+25delinsTTTC ENSP00000398305.2:n.2355+22_2355+25delins...
NM_001130455.1:c.2358+22_2358+25delinsTTTC NP_001123927.1:n.2358+22_2358+25delinsTTT...
NM_001130976.1:c.2313+22_2313+25delinsTTTC NP_001124448.1:n.2313+22_2313+25delinsTTT...
NM_001130977.1:c.2313+22_2313+25delinsTTTC NP_001124449.1:n.2313+22_2313+25delinsTTT...
NM_001130978.1:c.2355+22_2355+25delinsTTTC NP_001124450.1:n.2355+22_2355+25delinsTTT...
NM_001130979.1:c.2448+22_2448+25delinsTTTC NP_001124451.1:n.2448+22_2448+25delinsTTT...
NM_001130980.1:c.2406+22_2406+25delinsTTTC NP_001124452.1:n.2406+22_2406+25delinsTTT...
NM_001130981.1:c.2406+22_2406+25delinsTTTC NP_001124453.1:n.2406+22_2406+25delinsTTT...
NM_001130982.1:c.2451+22_2451+25delinsTTTC NP_001124454.1:n.2451+22_2451+25delinsTTT...
NM_001130983.1:c.2358+22_2358+25delinsTTTC NP_001124455.1:n.2358+22_2358+25delinsTTT...
NM_001130984.1:c.2316+22_2316+25delinsTTTC NP_001124456.1:n.2316+22_2316+25delinsTTT...
NM_001130985.1:c.2409+22_2409+25delinsTTTC NP_001124457.1:n.2409+22_2409+25delinsTTT...
NM_001130986.1:c.2316+22_2316+25delinsTTTC NP_001124458.1:n.2316+22_2316+25delinsTTT...
NM_001130987.1:c.2409+22_2409+25delinsTTTC NP_001124459.1:n.2409+22_2409+25delinsTTT...
NM_003494.3:c.2355+22_2355+25delinsTTTC NP_003485.1:n.2355+22_2355+25delinsTTTC
XM_005264584.3:c.2451+22_2451+25delinsTTTC XP_005264641.1:n.2451+22_2451+25delinsTTT...
XM_005264585.3:c.2448+22_2448+25delinsTTTC XP_005264642.1:n.2448+22_2448+25delinsTTT...
XM_005264584.4:c.2451+22_2451+25delinsTTTC XP_005264641.1:n.2451+22_2451+25delinsTTT...
XM_005264585.5:c.2448+22_2448+25delinsTTTC XP_005264642.1:n.2448+22_2448+25delinsTTT...
XR_001738969.1:n.2609+22_2609+25delinsTTTC
NM_001130987.2:c.2409+22_2409+25delinsTTTC MANE Select NP_001124459.1:n.2409+22_2409+25delinsTTT...
NM_001130455.2:c.2358+22_2358+25delinsTTTC NP_001123927.1:n.2358+22_2358+25delinsTTT...
NM_001130976.2:c.2313+22_2313+25delinsTTTC NP_001124448.1:n.2313+22_2313+25delinsTTT...
NM_001130977.2:c.2313+22_2313+25delinsTTTC NP_001124449.1:n.2313+22_2313+25delinsTTT...
NM_001130978.2:c.2355+22_2355+25delinsTTTC NP_001124450.1:n.2355+22_2355+25delinsTTT...
NM_001130979.2:c.2448+22_2448+25delinsTTTC NP_001124451.1:n.2448+22_2448+25delinsTTT...
NM_001130980.2:c.2406+22_2406+25delinsTTTC NP_001124452.1:n.2406+22_2406+25delinsTTT...
NM_001130981.2:c.2406+22_2406+25delinsTTTC NP_001124453.1:n.2406+22_2406+25delinsTTT...
NM_001130982.2:c.2451+22_2451+25delinsTTTC NP_001124454.1:n.2451+22_2451+25delinsTTT...
NM_001130983.2:c.2358+22_2358+25delinsTTTC NP_001124455.1:n.2358+22_2358+25delinsTTT...
NM_001130984.2:c.2316+22_2316+25delinsTTTC NP_001124456.1:n.2316+22_2316+25delinsTTT...
NM_001130985.2:c.2409+22_2409+25delinsTTTC NP_001124457.1:n.2409+22_2409+25delinsTTT...
NM_001130986.2:c.2316+22_2316+25delinsTTTC NP_001124458.1:n.2316+22_2316+25delinsTTT...
NM_003494.4:c.2355+22_2355+25delinsTTTC MANE Plus Clinical NP_003485.1:n.2355+22_2355+25delinsTTTC