Canonical Allele Identifier: CA1705886

Gene: DYSF

Linked Data

• dbSNP Id: rs766509442
• ExAC: 2:71778290 A / G
• gnomAD v2: 2-71778290-A-G
• gnomAD v4: 2-71551160-A-G
• MyVariant Identifiers: chr2:g.71778290A>G (hg19) ; chr2:g.71551160A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71551160A>G , CM000664.2:g.71551160A>G	GRCh38
NC_000002.11:g.71778290A>G , CM000664.1:g.71778290A>G	GRCh37
NC_000002.10:g.71631798A>G	NCBI36
NG_008694.1:g.102538A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258104.8:c.1638+4A>G MANE Plus Clinical	ENSP00000258104.3:n.1638+4A>G
ENST00000410020.8:c.1692+4A>G MANE Select	ENSP00000386881.3:n.1692+4A>G
ENST00000258104.7:c.1638+4A>G	ENSP00000258104.3:n.1638+4A>G
ENST00000394120.6:c.1641+4A>G	ENSP00000377678.2:n.1641+4A>G
ENST00000409366.5:c.1641+4A>G	ENSP00000386512.1:n.1641+4A>G
ENST00000409582.7:c.1689+4A>G	ENSP00000386547.3:n.1689+4A>G
ENST00000409651.5:c.1734+4A>G	ENSP00000386683.1:n.1734+4A>G
ENST00000409744.5:c.1599+4A>G	ENSP00000386285.1:n.1599+4A>G
ENST00000409762.5:c.1689+4A>G	ENSP00000387137.1:n.1689+4A>G
ENST00000410020.7:c.1692+4A>G	ENSP00000386881.3:n.1692+4A>G
ENST00000410041.1:c.1692+4A>G	ENSP00000386617.1:n.1692+4A>G
ENST00000413539.6:c.1731+4A>G	ENSP00000407046.2:n.1731+4A>G
ENST00000429174.6:c.1638+4A>G	ENSP00000398305.2:n.1638+4A>G
NM_001130455.1:c.1641+4A>G	NP_001123927.1:n.1641+4A>G
NM_001130976.1:c.1596+4A>G	NP_001124448.1:n.1596+4A>G
NM_001130977.1:c.1596+4A>G	NP_001124449.1:n.1596+4A>G
NM_001130978.1:c.1638+4A>G	NP_001124450.1:n.1638+4A>G
NM_001130979.1:c.1731+4A>G	NP_001124451.1:n.1731+4A>G
NM_001130980.1:c.1689+4A>G	NP_001124452.1:n.1689+4A>G
NM_001130981.1:c.1689+4A>G	NP_001124453.1:n.1689+4A>G
NM_001130982.1:c.1734+4A>G	NP_001124454.1:n.1734+4A>G
NM_001130983.1:c.1641+4A>G	NP_001124455.1:n.1641+4A>G
NM_001130984.1:c.1599+4A>G	NP_001124456.1:n.1599+4A>G
NM_001130985.1:c.1692+4A>G	NP_001124457.1:n.1692+4A>G
NM_001130986.1:c.1599+4A>G	NP_001124458.1:n.1599+4A>G
NM_001130987.1:c.1692+4A>G	NP_001124459.1:n.1692+4A>G
NM_003494.3:c.1638+4A>G	NP_003485.1:n.1638+4A>G
XM_005264584.3:c.1734+4A>G	XP_005264641.1:n.1734+4A>G
XM_005264585.3:c.1731+4A>G	XP_005264642.1:n.1731+4A>G
XM_005264584.4:c.1734+4A>G	XP_005264641.1:n.1734+4A>G
XM_005264585.5:c.1731+4A>G	XP_005264642.1:n.1731+4A>G
XR_001738969.1:n.1892+4A>G
NM_001130987.2:c.1692+4A>G MANE Select	NP_001124459.1:n.1692+4A>G
NM_001130455.2:c.1641+4A>G	NP_001123927.1:n.1641+4A>G
NM_001130976.2:c.1596+4A>G	NP_001124448.1:n.1596+4A>G
NM_001130977.2:c.1596+4A>G	NP_001124449.1:n.1596+4A>G
NM_001130978.2:c.1638+4A>G	NP_001124450.1:n.1638+4A>G
NM_001130979.2:c.1731+4A>G	NP_001124451.1:n.1731+4A>G
NM_001130980.2:c.1689+4A>G	NP_001124452.1:n.1689+4A>G
NM_001130981.2:c.1689+4A>G	NP_001124453.1:n.1689+4A>G
NM_001130982.2:c.1734+4A>G	NP_001124454.1:n.1734+4A>G
NM_001130983.2:c.1641+4A>G	NP_001124455.1:n.1641+4A>G
NM_001130984.2:c.1599+4A>G	NP_001124456.1:n.1599+4A>G
NM_001130985.2:c.1692+4A>G	NP_001124457.1:n.1692+4A>G
NM_001130986.2:c.1599+4A>G	NP_001124458.1:n.1599+4A>G
NM_003494.4:c.1638+4A>G MANE Plus Clinical	NP_003485.1:n.1638+4A>G