Canonical Allele Identifier: CA1707649

Gene: DYSF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71682574C>A , CM000664.2:g.71682574C>A	GRCh38
NC_000002.11:g.71909704C>A , CM000664.1:g.71909704C>A	GRCh37
NC_000002.10:g.71763212C>A	NCBI36
NG_008694.1:g.233952C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001130987.2:c.6218C>A MANE Select	NP_001124459.1:p.Thr2073Asn
ENST00000410020.8:c.6218C>A MANE Select	ENSP00000386881.3:p.Thr2073Asn
NM_003494.4:c.6101C>A MANE Plus Clinical	NP_003485.1:p.Thr2034Asn
ENST00000258104.8:c.6101C>A MANE Plus Clinical	ENSP00000258104.3:p.Thr2034Asn
NM_001130455.1:c.6104C>A	NP_001123927.1:p.Thr2035Asn
NM_001130455.2:c.6104C>A	NP_001123927.1:p.Thr2035Asn
NM_001130976.1:c.6059C>A	NP_001124448.1:p.Thr2020Asn
NM_001130976.2:c.6059C>A	NP_001124448.1:p.Thr2020Asn
NM_001130977.1:c.6122C>A	NP_001124449.1:p.Thr2041Asn
NM_001130977.2:c.6122C>A	NP_001124449.1:p.Thr2041Asn
NM_001130978.1:c.6164C>A	NP_001124450.1:p.Thr2055Asn
NM_001130978.2:c.6164C>A	NP_001124450.1:p.Thr2055Asn
NM_001130979.1:c.6194C>A	NP_001124451.1:p.Thr2065Asn
NM_001130979.2:c.6194C>A	NP_001124451.1:p.Thr2065Asn
NM_001130980.1:c.6152C>A	NP_001124452.1:p.Thr2051Asn
NM_001130980.2:c.6152C>A	NP_001124452.1:p.Thr2051Asn
NM_001130981.1:c.6215C>A	NP_001124453.1:p.Thr2072Asn
NM_001130981.2:c.6215C>A	NP_001124453.1:p.Thr2072Asn
NM_001130982.1:c.6197C>A	NP_001124454.1:p.Thr2066Asn
NM_001130982.2:c.6197C>A	NP_001124454.1:p.Thr2066Asn
NM_001130983.1:c.6167C>A	NP_001124455.1:p.Thr2056Asn
NM_001130983.2:c.6167C>A	NP_001124455.1:p.Thr2056Asn
NM_001130984.1:c.6125C>A	NP_001124456.1:p.Thr2042Asn
NM_001130984.2:c.6125C>A	NP_001124456.1:p.Thr2042Asn
NM_001130985.1:c.6155C>A	NP_001124457.1:p.Thr2052Asn
NM_001130985.2:c.6155C>A	NP_001124457.1:p.Thr2052Asn
NM_001130986.1:c.6062C>A	NP_001124458.1:p.Thr2021Asn
NM_001130986.2:c.6062C>A	NP_001124458.1:p.Thr2021Asn
NM_001130987.1:c.6218C>A	NP_001124459.1:p.Thr2073Asn
NM_003494.3:c.6101C>A	NP_003485.1:p.Thr2034Asn
ENST00000258104.7:c.6101C>A	ENSP00000258104.3:p.Thr2034Asn
ENST00000394120.6:c.6104C>A	ENSP00000377678.2:p.Thr2035Asn
ENST00000409366.5:c.6167C>A	ENSP00000386512.1:p.Thr2056Asn
ENST00000409582.7:c.6215C>A	ENSP00000386547.3:p.Thr2072Asn
ENST00000409651.5:c.6197C>A	ENSP00000386683.1:p.Thr2066Asn
ENST00000409744.5:c.6125C>A	ENSP00000386285.1:p.Thr2042Asn
ENST00000409762.5:c.6152C>A	ENSP00000387137.1:p.Thr2051Asn
ENST00000410020.7:c.6218C>A	ENSP00000386881.3:p.Thr2073Asn
ENST00000410041.1:c.6155C>A	ENSP00000386617.1:p.Thr2052Asn
ENST00000413539.6:c.6194C>A	ENSP00000407046.2:p.Thr2065Asn
ENST00000429174.6:c.6164C>A	ENSP00000398305.2:p.Thr2055Asn
ENST00000479049.6:n.2986C>A
ENST00000698057.1:c.3632C>A	ENSP00000513536.1:p.Thr1211Asn
ENST00000698058.1:c.2849C>A	ENSP00000513537.1:p.Thr950Asn
ENST00000698059.1:c.2957C>A	ENSP00000513538.1:p.Thr986Asn
XM_005264584.3:c.6260C>A	XP_005264641.1:p.Thr2087Asn
XM_005264584.4:c.6260C>A	XP_005264641.1:p.Thr2087Asn
XM_005264585.3:c.6257C>A	XP_005264642.1:p.Thr2086Asn
XM_005264585.5:c.6257C>A	XP_005264642.1:p.Thr2086Asn