Canonical Allele Identifier: CA347226557

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71906339G>T (hg19) ; chr2:g.71679209G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71679209G>T , CM000664.2:g.71679209G>T	GRCh38
NC_000002.11:g.71906339G>T , CM000664.1:g.71906339G>T	GRCh37
NC_000002.10:g.71759847G>T	NCBI36
NG_008694.1:g.230587G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698057.1:c.3451G>T	ENSP00000513536.1:p.Glu1151Ter
ENST00000698058.1:c.2668G>T	ENSP00000513537.1:p.Glu890Ter
ENST00000698059.1:c.2776G>T	ENSP00000513538.1:p.Glu926Ter
ENST00000258104.8:c.5920G>T MANE Plus Clinical	ENSP00000258104.3:p.Glu1974Ter
ENST00000410020.8:c.6037G>T MANE Select	ENSP00000386881.3:p.Glu2013Ter
ENST00000258104.7:c.5920G>T	ENSP00000258104.3:p.Glu1974Ter
ENST00000394120.6:c.5923G>T	ENSP00000377678.2:p.Glu1975Ter
ENST00000409366.5:c.5986G>T	ENSP00000386512.1:p.Glu1996Ter
ENST00000409582.7:c.6034G>T	ENSP00000386547.3:p.Glu2012Ter
ENST00000409651.5:c.6016G>T	ENSP00000386683.1:p.Glu2006Ter
ENST00000409744.5:c.5944G>T	ENSP00000386285.1:p.Glu1982Ter
ENST00000409762.5:c.5971G>T	ENSP00000387137.1:p.Glu1991Ter
ENST00000410020.7:c.6037G>T	ENSP00000386881.3:p.Glu2013Ter
ENST00000410041.1:c.5974G>T	ENSP00000386617.1:p.Glu1992Ter
ENST00000413539.6:c.6013G>T	ENSP00000407046.2:p.Glu2005Ter
ENST00000429174.6:c.5983G>T	ENSP00000398305.2:p.Glu1995Ter
ENST00000479049.6:n.2805G>T
NM_001130455.1:c.5923G>T	NP_001123927.1:p.Glu1975Ter
NM_001130976.1:c.5878G>T	NP_001124448.1:p.Glu1960Ter
NM_001130977.1:c.5941G>T	NP_001124449.1:p.Glu1981Ter
NM_001130978.1:c.5983G>T	NP_001124450.1:p.Glu1995Ter
NM_001130979.1:c.6013G>T	NP_001124451.1:p.Glu2005Ter
NM_001130980.1:c.5971G>T	NP_001124452.1:p.Glu1991Ter
NM_001130981.1:c.6034G>T	NP_001124453.1:p.Glu2012Ter
NM_001130982.1:c.6016G>T	NP_001124454.1:p.Glu2006Ter
NM_001130983.1:c.5986G>T	NP_001124455.1:p.Glu1996Ter
NM_001130984.1:c.5944G>T	NP_001124456.1:p.Glu1982Ter
NM_001130985.1:c.5974G>T	NP_001124457.1:p.Glu1992Ter
NM_001130986.1:c.5881G>T	NP_001124458.1:p.Glu1961Ter
NM_001130987.1:c.6037G>T	NP_001124459.1:p.Glu2013Ter
NM_003494.3:c.5920G>T	NP_003485.1:p.Glu1974Ter
XM_005264584.3:c.6079G>T	XP_005264641.1:p.Glu2027Ter
XM_005264585.3:c.6076G>T	XP_005264642.1:p.Glu2026Ter
XM_005264584.4:c.6079G>T	XP_005264641.1:p.Glu2027Ter
XM_005264585.5:c.6076G>T	XP_005264642.1:p.Glu2026Ter
NM_001130987.2:c.6037G>T MANE Select	NP_001124459.1:p.Glu2013Ter
NM_001130455.2:c.5923G>T	NP_001123927.1:p.Glu1975Ter
NM_001130976.2:c.5878G>T	NP_001124448.1:p.Glu1960Ter
NM_001130977.2:c.5941G>T	NP_001124449.1:p.Glu1981Ter
NM_001130978.2:c.5983G>T	NP_001124450.1:p.Glu1995Ter
NM_001130979.2:c.6013G>T	NP_001124451.1:p.Glu2005Ter
NM_001130980.2:c.5971G>T	NP_001124452.1:p.Glu1991Ter
NM_001130981.2:c.6034G>T	NP_001124453.1:p.Glu2012Ter
NM_001130982.2:c.6016G>T	NP_001124454.1:p.Glu2006Ter
NM_001130983.2:c.5986G>T	NP_001124455.1:p.Glu1996Ter
NM_001130984.2:c.5944G>T	NP_001124456.1:p.Glu1982Ter
NM_001130985.2:c.5974G>T	NP_001124457.1:p.Glu1992Ter
NM_001130986.2:c.5881G>T	NP_001124458.1:p.Glu1961Ter
NM_003494.4:c.5920G>T MANE Plus Clinical	NP_003485.1:p.Glu1974Ter