Canonical Allele Identifier: CA347226525

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71906328C>G (hg19) ; chr2:g.71679198C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71679198C>G , CM000664.2:g.71679198C>G	GRCh38
NC_000002.11:g.71906328C>G , CM000664.1:g.71906328C>G	GRCh37
NC_000002.10:g.71759836C>G	NCBI36
NG_008694.1:g.230576C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698057.1:c.3440C>G	ENSP00000513536.1:p.Pro1147Arg
ENST00000698058.1:c.2657C>G	ENSP00000513537.1:p.Pro886Arg
ENST00000698059.1:c.2765C>G	ENSP00000513538.1:p.Pro922Arg
ENST00000258104.8:c.5909C>G MANE Plus Clinical	ENSP00000258104.3:p.Pro1970Arg
ENST00000410020.8:c.6026C>G MANE Select	ENSP00000386881.3:p.Pro2009Arg
ENST00000258104.7:c.5909C>G	ENSP00000258104.3:p.Pro1970Arg
ENST00000394120.6:c.5912C>G	ENSP00000377678.2:p.Pro1971Arg
ENST00000409366.5:c.5975C>G	ENSP00000386512.1:p.Pro1992Arg
ENST00000409582.7:c.6023C>G	ENSP00000386547.3:p.Pro2008Arg
ENST00000409651.5:c.6005C>G	ENSP00000386683.1:p.Pro2002Arg
ENST00000409744.5:c.5933C>G	ENSP00000386285.1:p.Pro1978Arg
ENST00000409762.5:c.5960C>G	ENSP00000387137.1:p.Pro1987Arg
ENST00000410020.7:c.6026C>G	ENSP00000386881.3:p.Pro2009Arg
ENST00000410041.1:c.5963C>G	ENSP00000386617.1:p.Pro1988Arg
ENST00000413539.6:c.6002C>G	ENSP00000407046.2:p.Pro2001Arg
ENST00000429174.6:c.5972C>G	ENSP00000398305.2:p.Pro1991Arg
ENST00000479049.6:n.2794C>G
NM_001130455.1:c.5912C>G	NP_001123927.1:p.Pro1971Arg
NM_001130976.1:c.5867C>G	NP_001124448.1:p.Pro1956Arg
NM_001130977.1:c.5930C>G	NP_001124449.1:p.Pro1977Arg
NM_001130978.1:c.5972C>G	NP_001124450.1:p.Pro1991Arg
NM_001130979.1:c.6002C>G	NP_001124451.1:p.Pro2001Arg
NM_001130980.1:c.5960C>G	NP_001124452.1:p.Pro1987Arg
NM_001130981.1:c.6023C>G	NP_001124453.1:p.Pro2008Arg
NM_001130982.1:c.6005C>G	NP_001124454.1:p.Pro2002Arg
NM_001130983.1:c.5975C>G	NP_001124455.1:p.Pro1992Arg
NM_001130984.1:c.5933C>G	NP_001124456.1:p.Pro1978Arg
NM_001130985.1:c.5963C>G	NP_001124457.1:p.Pro1988Arg
NM_001130986.1:c.5870C>G	NP_001124458.1:p.Pro1957Arg
NM_001130987.1:c.6026C>G	NP_001124459.1:p.Pro2009Arg
NM_003494.3:c.5909C>G	NP_003485.1:p.Pro1970Arg
XM_005264584.3:c.6068C>G	XP_005264641.1:p.Pro2023Arg
XM_005264585.3:c.6065C>G	XP_005264642.1:p.Pro2022Arg
XM_005264584.4:c.6068C>G	XP_005264641.1:p.Pro2023Arg
XM_005264585.5:c.6065C>G	XP_005264642.1:p.Pro2022Arg
NM_001130987.2:c.6026C>G MANE Select	NP_001124459.1:p.Pro2009Arg
NM_001130455.2:c.5912C>G	NP_001123927.1:p.Pro1971Arg
NM_001130976.2:c.5867C>G	NP_001124448.1:p.Pro1956Arg
NM_001130977.2:c.5930C>G	NP_001124449.1:p.Pro1977Arg
NM_001130978.2:c.5972C>G	NP_001124450.1:p.Pro1991Arg
NM_001130979.2:c.6002C>G	NP_001124451.1:p.Pro2001Arg
NM_001130980.2:c.5960C>G	NP_001124452.1:p.Pro1987Arg
NM_001130981.2:c.6023C>G	NP_001124453.1:p.Pro2008Arg
NM_001130982.2:c.6005C>G	NP_001124454.1:p.Pro2002Arg
NM_001130983.2:c.5975C>G	NP_001124455.1:p.Pro1992Arg
NM_001130984.2:c.5933C>G	NP_001124456.1:p.Pro1978Arg
NM_001130985.2:c.5963C>G	NP_001124457.1:p.Pro1988Arg
NM_001130986.2:c.5870C>G	NP_001124458.1:p.Pro1957Arg
NM_003494.4:c.5909C>G MANE Plus Clinical	NP_003485.1:p.Pro1970Arg