Canonical Allele Identifier: CA1260095598
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71552971_71552972delinsTG , CM000664.2:g.71552971_71552972delinsTG GRCh38
NC_000002.11:g.71780101_71780102delinsTG , CM000664.1:g.71780101_71780102delinsTG GRCh37
NC_000002.10:g.71633609_71633610delinsTG NCBI36
NG_008694.1:g.104349_104350delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000258104.8:c.1753-40_1753-39delinsTG MANE Plus Clinical ENSP00000258104.3:n.1753-40_1753-39delins...
ENST00000410020.8:c.1807-40_1807-39delinsTG MANE Select ENSP00000386881.3:n.1807-40_1807-39delins...
ENST00000258104.7:c.1753-40_1753-39delinsTG ENSP00000258104.3:n.1753-40_1753-39delins...
ENST00000394120.6:c.1756-40_1756-39delinsTG ENSP00000377678.2:n.1756-40_1756-39delins...
ENST00000409366.5:c.1756-40_1756-39delinsTG ENSP00000386512.1:n.1756-40_1756-39delins...
ENST00000409582.7:c.1804-40_1804-39delinsTG ENSP00000386547.3:n.1804-40_1804-39delins...
ENST00000409651.5:c.1849-40_1849-39delinsTG ENSP00000386683.1:n.1849-40_1849-39delins...
ENST00000409744.5:c.1714-40_1714-39delinsTG ENSP00000386285.1:n.1714-40_1714-39delins...
ENST00000409762.5:c.1804-40_1804-39delinsTG ENSP00000387137.1:n.1804-40_1804-39delins...
ENST00000410020.7:c.1807-40_1807-39delinsTG ENSP00000386881.3:n.1807-40_1807-39delins...
ENST00000410041.1:c.1807-40_1807-39delinsTG ENSP00000386617.1:n.1807-40_1807-39delins...
ENST00000413539.6:c.1846-40_1846-39delinsTG ENSP00000407046.2:n.1846-40_1846-39delins...
ENST00000429174.6:c.1753-40_1753-39delinsTG ENSP00000398305.2:n.1753-40_1753-39delins...
NM_001130455.1:c.1756-40_1756-39delinsTG NP_001123927.1:n.1756-40_1756-39delinsTG
NM_001130976.1:c.1711-40_1711-39delinsTG NP_001124448.1:n.1711-40_1711-39delinsTG
NM_001130977.1:c.1711-40_1711-39delinsTG NP_001124449.1:n.1711-40_1711-39delinsTG
NM_001130978.1:c.1753-40_1753-39delinsTG NP_001124450.1:n.1753-40_1753-39delinsTG
NM_001130979.1:c.1846-40_1846-39delinsTG NP_001124451.1:n.1846-40_1846-39delinsTG
NM_001130980.1:c.1804-40_1804-39delinsTG NP_001124452.1:n.1804-40_1804-39delinsTG
NM_001130981.1:c.1804-40_1804-39delinsTG NP_001124453.1:n.1804-40_1804-39delinsTG
NM_001130982.1:c.1849-40_1849-39delinsTG NP_001124454.1:n.1849-40_1849-39delinsTG
NM_001130983.1:c.1756-40_1756-39delinsTG NP_001124455.1:n.1756-40_1756-39delinsTG
NM_001130984.1:c.1714-40_1714-39delinsTG NP_001124456.1:n.1714-40_1714-39delinsTG
NM_001130985.1:c.1807-40_1807-39delinsTG NP_001124457.1:n.1807-40_1807-39delinsTG
NM_001130986.1:c.1714-40_1714-39delinsTG NP_001124458.1:n.1714-40_1714-39delinsTG
NM_001130987.1:c.1807-40_1807-39delinsTG NP_001124459.1:n.1807-40_1807-39delinsTG
NM_003494.3:c.1753-40_1753-39delinsTG NP_003485.1:n.1753-40_1753-39delinsTG
XM_005264584.3:c.1849-40_1849-39delinsTG XP_005264641.1:n.1849-40_1849-39delinsTG
XM_005264585.3:c.1846-40_1846-39delinsTG XP_005264642.1:n.1846-40_1846-39delinsTG
XM_005264584.4:c.1849-40_1849-39delinsTG XP_005264641.1:n.1849-40_1849-39delinsTG
XM_005264585.5:c.1846-40_1846-39delinsTG XP_005264642.1:n.1846-40_1846-39delinsTG
XR_001738969.1:n.2007-40_2007-39delinsTG
NM_001130987.2:c.1807-40_1807-39delinsTG MANE Select NP_001124459.1:n.1807-40_1807-39delinsTG
NM_001130455.2:c.1756-40_1756-39delinsTG NP_001123927.1:n.1756-40_1756-39delinsTG
NM_001130976.2:c.1711-40_1711-39delinsTG NP_001124448.1:n.1711-40_1711-39delinsTG
NM_001130977.2:c.1711-40_1711-39delinsTG NP_001124449.1:n.1711-40_1711-39delinsTG
NM_001130978.2:c.1753-40_1753-39delinsTG NP_001124450.1:n.1753-40_1753-39delinsTG
NM_001130979.2:c.1846-40_1846-39delinsTG NP_001124451.1:n.1846-40_1846-39delinsTG
NM_001130980.2:c.1804-40_1804-39delinsTG NP_001124452.1:n.1804-40_1804-39delinsTG
NM_001130981.2:c.1804-40_1804-39delinsTG NP_001124453.1:n.1804-40_1804-39delinsTG
NM_001130982.2:c.1849-40_1849-39delinsTG NP_001124454.1:n.1849-40_1849-39delinsTG
NM_001130983.2:c.1756-40_1756-39delinsTG NP_001124455.1:n.1756-40_1756-39delinsTG
NM_001130984.2:c.1714-40_1714-39delinsTG NP_001124456.1:n.1714-40_1714-39delinsTG
NM_001130985.2:c.1807-40_1807-39delinsTG NP_001124457.1:n.1807-40_1807-39delinsTG
NM_001130986.2:c.1714-40_1714-39delinsTG NP_001124458.1:n.1714-40_1714-39delinsTG
NM_003494.4:c.1753-40_1753-39delinsTG MANE Plus Clinical NP_003485.1:n.1753-40_1753-39delinsTG