Canonical Allele Identifier: CA347227891

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71913605G>T (hg19) ; chr2:g.71686475G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71686475G>T , CM000664.2:g.71686475G>T	GRCh38
NC_000002.11:g.71913605G>T , CM000664.1:g.71913605G>T	GRCh37
NC_000002.10:g.71767113G>T	NCBI36
NG_008694.1:g.237853G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3757G>T	ENSP00000513536.1:p.Val1253Leu
ENST00000698058.1:c.2974G>T	ENSP00000513537.1:p.Val992Leu
ENST00000698059.1:c.3082G>T	ENSP00000513538.1:p.Val1028Leu
ENST00000258104.8:c.6226G>T MANE Plus Clinical	ENSP00000258104.3:p.Val2076Leu
ENST00000410020.8:c.6343G>T MANE Select	ENSP00000386881.3:p.Val2115Leu
ENST00000258104.7:c.6226G>T	ENSP00000258104.3:p.Val2076Leu
ENST00000394120.6:c.6229G>T	ENSP00000377678.2:p.Val2077Leu
ENST00000409366.5:c.6292G>T	ENSP00000386512.1:p.Val2098Leu
ENST00000409582.7:c.6340G>T	ENSP00000386547.3:p.Val2114Leu
ENST00000409651.5:c.6322G>T	ENSP00000386683.1:p.Val2108Leu
ENST00000409744.5:c.6250G>T	ENSP00000386285.1:p.Val2084Leu
ENST00000409762.5:c.6277G>T	ENSP00000387137.1:p.Val2093Leu
ENST00000410020.7:c.6343G>T	ENSP00000386881.3:p.Val2115Leu
ENST00000410041.1:c.6280G>T	ENSP00000386617.1:p.Val2094Leu
ENST00000413539.6:c.6319G>T	ENSP00000407046.2:p.Val2107Leu
ENST00000429174.6:c.6289G>T	ENSP00000398305.2:p.Val2097Leu
ENST00000479049.6:n.3111G>T
NM_001130455.1:c.6229G>T	NP_001123927.1:p.Val2077Leu
NM_001130976.1:c.6184G>T	NP_001124448.1:p.Val2062Leu
NM_001130977.1:c.6247G>T	NP_001124449.1:p.Val2083Leu
NM_001130978.1:c.6289G>T	NP_001124450.1:p.Val2097Leu
NM_001130979.1:c.6319G>T	NP_001124451.1:p.Val2107Leu
NM_001130980.1:c.6277G>T	NP_001124452.1:p.Val2093Leu
NM_001130981.1:c.6340G>T	NP_001124453.1:p.Val2114Leu
NM_001130982.1:c.6322G>T	NP_001124454.1:p.Val2108Leu
NM_001130983.1:c.6292G>T	NP_001124455.1:p.Val2098Leu
NM_001130984.1:c.6250G>T	NP_001124456.1:p.Val2084Leu
NM_001130985.1:c.6280G>T	NP_001124457.1:p.Val2094Leu
NM_001130986.1:c.6187G>T	NP_001124458.1:p.Val2063Leu
NM_001130987.1:c.6343G>T	NP_001124459.1:p.Val2115Leu
NM_003494.3:c.6226G>T	NP_003485.1:p.Val2076Leu
XM_005264584.3:c.6385G>T	XP_005264641.1:p.Val2129Leu
XM_005264585.3:c.6382G>T	XP_005264642.1:p.Val2128Leu
XM_005264584.4:c.6385G>T	XP_005264641.1:p.Val2129Leu
XM_005264585.5:c.6382G>T	XP_005264642.1:p.Val2128Leu
NM_001130987.2:c.6343G>T MANE Select	NP_001124459.1:p.Val2115Leu
NM_001130455.2:c.6229G>T	NP_001123927.1:p.Val2077Leu
NM_001130976.2:c.6184G>T	NP_001124448.1:p.Val2062Leu
NM_001130977.2:c.6247G>T	NP_001124449.1:p.Val2083Leu
NM_001130978.2:c.6289G>T	NP_001124450.1:p.Val2097Leu
NM_001130979.2:c.6319G>T	NP_001124451.1:p.Val2107Leu
NM_001130980.2:c.6277G>T	NP_001124452.1:p.Val2093Leu
NM_001130981.2:c.6340G>T	NP_001124453.1:p.Val2114Leu
NM_001130982.2:c.6322G>T	NP_001124454.1:p.Val2108Leu
NM_001130983.2:c.6292G>T	NP_001124455.1:p.Val2098Leu
NM_001130984.2:c.6250G>T	NP_001124456.1:p.Val2084Leu
NM_001130985.2:c.6280G>T	NP_001124457.1:p.Val2094Leu
NM_001130986.2:c.6187G>T	NP_001124458.1:p.Val2063Leu
NM_003494.4:c.6226G>T MANE Plus Clinical	NP_003485.1:p.Val2076Leu