Canonical Allele Identifier: CA347227937

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71913622A>G (hg19) ; chr2:g.71686492A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71686492A>G , CM000664.2:g.71686492A>G	GRCh38
NC_000002.11:g.71913622A>G , CM000664.1:g.71913622A>G	GRCh37
NC_000002.10:g.71767130A>G	NCBI36
NG_008694.1:g.237870A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3774A>G	ENSP00000513536.1:p.Ter1258Trp
ENST00000698058.1:c.2991A>G	ENSP00000513537.1:p.Ter997Trp
ENST00000698059.1:c.3099A>G	ENSP00000513538.1:p.Ter1033Trp
ENST00000258104.8:c.6243A>G MANE Plus Clinical	ENSP00000258104.3:p.Ter2081Trp
ENST00000410020.8:c.6360A>G MANE Select	ENSP00000386881.3:p.Ter2120Trp
ENST00000258104.7:c.6243A>G	ENSP00000258104.3:p.Ter2081Trp
ENST00000394120.6:c.6246A>G	ENSP00000377678.2:p.Ter2082Trp
ENST00000409366.5:c.6309A>G	ENSP00000386512.1:p.Ter2103Trp
ENST00000409582.7:c.6357A>G	ENSP00000386547.3:p.Ter2119Trp
ENST00000409651.5:c.6339A>G	ENSP00000386683.1:p.Ter2113Trp
ENST00000409744.5:c.6267A>G	ENSP00000386285.1:p.Ter2089Trp
ENST00000409762.5:c.6294A>G	ENSP00000387137.1:p.Ter2098Trp
ENST00000410020.7:c.6360A>G	ENSP00000386881.3:p.Ter2120Trp
ENST00000410041.1:c.6297A>G	ENSP00000386617.1:p.Ter2099Trp
ENST00000413539.6:c.6336A>G	ENSP00000407046.2:p.Ter2112Trp
ENST00000429174.6:c.6306A>G	ENSP00000398305.2:p.Ter2102Trp
ENST00000479049.6:n.3128A>G
NM_001130455.1:c.6246A>G	NP_001123927.1:p.Ter2082Trp
NM_001130976.1:c.6201A>G	NP_001124448.1:p.Ter2067Trp
NM_001130977.1:c.6264A>G	NP_001124449.1:p.Ter2088Trp
NM_001130978.1:c.6306A>G	NP_001124450.1:p.Ter2102Trp
NM_001130979.1:c.6336A>G	NP_001124451.1:p.Ter2112Trp
NM_001130980.1:c.6294A>G	NP_001124452.1:p.Ter2098Trp
NM_001130981.1:c.6357A>G	NP_001124453.1:p.Ter2119Trp
NM_001130982.1:c.6339A>G	NP_001124454.1:p.Ter2113Trp
NM_001130983.1:c.6309A>G	NP_001124455.1:p.Ter2103Trp
NM_001130984.1:c.6267A>G	NP_001124456.1:p.Ter2089Trp
NM_001130985.1:c.6297A>G	NP_001124457.1:p.Ter2099Trp
NM_001130986.1:c.6204A>G	NP_001124458.1:p.Ter2068Trp
NM_001130987.1:c.6360A>G	NP_001124459.1:p.Ter2120Trp
NM_003494.3:c.6243A>G	NP_003485.1:p.Ter2081Trp
XM_005264584.3:c.6402A>G	XP_005264641.1:p.Ter2134Trp
XM_005264585.3:c.6399A>G	XP_005264642.1:p.Ter2133Trp
XM_005264584.4:c.6402A>G	XP_005264641.1:p.Ter2134Trp
XM_005264585.5:c.6399A>G	XP_005264642.1:p.Ter2133Trp
NM_001130987.2:c.6360A>G MANE Select	NP_001124459.1:p.Ter2120Trp
NM_001130455.2:c.6246A>G	NP_001123927.1:p.Ter2082Trp
NM_001130976.2:c.6201A>G	NP_001124448.1:p.Ter2067Trp
NM_001130977.2:c.6264A>G	NP_001124449.1:p.Ter2088Trp
NM_001130978.2:c.6306A>G	NP_001124450.1:p.Ter2102Trp
NM_001130979.2:c.6336A>G	NP_001124451.1:p.Ter2112Trp
NM_001130980.2:c.6294A>G	NP_001124452.1:p.Ter2098Trp
NM_001130981.2:c.6357A>G	NP_001124453.1:p.Ter2119Trp
NM_001130982.2:c.6339A>G	NP_001124454.1:p.Ter2113Trp
NM_001130983.2:c.6309A>G	NP_001124455.1:p.Ter2103Trp
NM_001130984.2:c.6267A>G	NP_001124456.1:p.Ter2089Trp
NM_001130985.2:c.6297A>G	NP_001124457.1:p.Ter2099Trp
NM_001130986.2:c.6204A>G	NP_001124458.1:p.Ter2068Trp
NM_003494.4:c.6243A>G MANE Plus Clinical	NP_003485.1:p.Ter2081Trp