Canonical Allele Identifier: CA347226635

Gene: DYSF

Linked Data

• dbSNP Id: rs1299489202
• gnomAD v2: 2-71829922-G-A
• gnomAD v3: 2-71602792-G-A
• gnomAD v4: 2-71602792-G-A
• MyVariant Identifiers: chr2:g.71829922G>A (hg19) ; chr2:g.71602792G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71602792G>A , CM000664.2:g.71602792G>A	GRCh38
NC_000002.11:g.71829922G>A , CM000664.1:g.71829922G>A	GRCh37
NC_000002.10:g.71683430G>A	NCBI36
NG_008694.1:g.154170G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.1316G>A	ENSP00000513536.1:p.Arg439Lys
ENST00000698058.1:c.533G>A	ENSP00000513537.1:p.Arg178Lys
ENST00000698059.1:c.533G>A	ENSP00000513538.1:p.Arg178Lys
ENST00000258104.8:c.3890G>A MANE Plus Clinical	ENSP00000258104.3:p.Arg1297Lys
ENST00000410020.8:c.3944G>A MANE Select	ENSP00000386881.3:p.Arg1315Lys
ENST00000258104.7:c.3890G>A	ENSP00000258104.3:p.Arg1297Lys
ENST00000394120.6:c.3893G>A	ENSP00000377678.2:p.Arg1298Lys
ENST00000409366.5:c.3893G>A	ENSP00000386512.1:p.Arg1298Lys
ENST00000409582.7:c.3941G>A	ENSP00000386547.3:p.Arg1314Lys
ENST00000409651.5:c.3986G>A	ENSP00000386683.1:p.Arg1329Lys
ENST00000409744.5:c.3851G>A	ENSP00000386285.1:p.Arg1284Lys
ENST00000409762.5:c.3941G>A	ENSP00000387137.1:p.Arg1314Lys
ENST00000410020.7:c.3944G>A	ENSP00000386881.3:p.Arg1315Lys
ENST00000410041.1:c.3944G>A	ENSP00000386617.1:p.Arg1315Lys
ENST00000413539.6:c.3983G>A	ENSP00000407046.2:p.Arg1328Lys
ENST00000429174.6:c.3890G>A	ENSP00000398305.2:p.Arg1297Lys
ENST00000472873.5:n.274G>A
ENST00000479049.6:n.775G>A
ENST00000487180.5:n.109G>A
ENST00000494501.5:n.250G>A
NM_001130455.1:c.3893G>A	NP_001123927.1:p.Arg1298Lys
NM_001130976.1:c.3848G>A	NP_001124448.1:p.Arg1283Lys
NM_001130977.1:c.3848G>A	NP_001124449.1:p.Arg1283Lys
NM_001130978.1:c.3890G>A	NP_001124450.1:p.Arg1297Lys
NM_001130979.1:c.3983G>A	NP_001124451.1:p.Arg1328Lys
NM_001130980.1:c.3941G>A	NP_001124452.1:p.Arg1314Lys
NM_001130981.1:c.3941G>A	NP_001124453.1:p.Arg1314Lys
NM_001130982.1:c.3986G>A	NP_001124454.1:p.Arg1329Lys
NM_001130983.1:c.3893G>A	NP_001124455.1:p.Arg1298Lys
NM_001130984.1:c.3851G>A	NP_001124456.1:p.Arg1284Lys
NM_001130985.1:c.3944G>A	NP_001124457.1:p.Arg1315Lys
NM_001130986.1:c.3851G>A	NP_001124458.1:p.Arg1284Lys
NM_001130987.1:c.3944G>A	NP_001124459.1:p.Arg1315Lys
NM_003494.3:c.3890G>A	NP_003485.1:p.Arg1297Lys
XM_005264584.3:c.3986G>A	XP_005264641.1:p.Arg1329Lys
XM_005264585.3:c.3983G>A	XP_005264642.1:p.Arg1328Lys
XM_005264584.4:c.3986G>A	XP_005264641.1:p.Arg1329Lys
XM_005264585.5:c.3983G>A	XP_005264642.1:p.Arg1328Lys
XR_001738969.1:n.4144G>A
NM_001130987.2:c.3944G>A MANE Select	NP_001124459.1:p.Arg1315Lys
NM_001130455.2:c.3893G>A	NP_001123927.1:p.Arg1298Lys
NM_001130976.2:c.3848G>A	NP_001124448.1:p.Arg1283Lys
NM_001130977.2:c.3848G>A	NP_001124449.1:p.Arg1283Lys
NM_001130978.2:c.3890G>A	NP_001124450.1:p.Arg1297Lys
NM_001130979.2:c.3983G>A	NP_001124451.1:p.Arg1328Lys
NM_001130980.2:c.3941G>A	NP_001124452.1:p.Arg1314Lys
NM_001130981.2:c.3941G>A	NP_001124453.1:p.Arg1314Lys
NM_001130982.2:c.3986G>A	NP_001124454.1:p.Arg1329Lys
NM_001130983.2:c.3893G>A	NP_001124455.1:p.Arg1298Lys
NM_001130984.2:c.3851G>A	NP_001124456.1:p.Arg1284Lys
NM_001130985.2:c.3944G>A	NP_001124457.1:p.Arg1315Lys
NM_001130986.2:c.3851G>A	NP_001124458.1:p.Arg1284Lys
NM_003494.4:c.3890G>A MANE Plus Clinical	NP_003485.1:p.Arg1297Lys