Canonical Allele Identifier: CA347216925

Gene: DYSF

Linked Data

• dbSNP Id: rs1559185322
• gnomAD v2: 2-71797746-A-G
• gnomAD v4: 2-71570616-A-G
• MyVariant Identifiers: chr2:g.71797746A>G (hg19) ; chr2:g.71570616A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71570616A>G , CM000664.2:g.71570616A>G	GRCh38
NC_000002.11:g.71797746A>G , CM000664.1:g.71797746A>G	GRCh37
NC_000002.10:g.71651254A>G	NCBI36
NG_008694.1:g.121994A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.475A>G	ENSP00000513536.1:p.Thr159Ala
ENST00000258104.8:c.3049A>G MANE Plus Clinical	ENSP00000258104.3:p.Thr1017Ala
ENST00000410020.8:c.3103A>G MANE Select	ENSP00000386881.3:p.Thr1035Ala
ENST00000258104.7:c.3049A>G	ENSP00000258104.3:p.Thr1017Ala
ENST00000394120.6:c.3052A>G	ENSP00000377678.2:p.Thr1018Ala
ENST00000409366.5:c.3052A>G	ENSP00000386512.1:p.Thr1018Ala
ENST00000409582.7:c.3100A>G	ENSP00000386547.3:p.Thr1034Ala
ENST00000409651.5:c.3145A>G	ENSP00000386683.1:p.Thr1049Ala
ENST00000409744.5:c.3010A>G	ENSP00000386285.1:p.Thr1004Ala
ENST00000409762.5:c.3100A>G	ENSP00000387137.1:p.Thr1034Ala
ENST00000410020.7:c.3103A>G	ENSP00000386881.3:p.Thr1035Ala
ENST00000410041.1:c.3103A>G	ENSP00000386617.1:p.Thr1035Ala
ENST00000413539.6:c.3142A>G	ENSP00000407046.2:p.Thr1048Ala
ENST00000429174.6:c.3049A>G	ENSP00000398305.2:p.Thr1017Ala
ENST00000461565.1:n.215A>G
NM_001130455.1:c.3052A>G	NP_001123927.1:p.Thr1018Ala
NM_001130976.1:c.3007A>G	NP_001124448.1:p.Thr1003Ala
NM_001130977.1:c.3007A>G	NP_001124449.1:p.Thr1003Ala
NM_001130978.1:c.3049A>G	NP_001124450.1:p.Thr1017Ala
NM_001130979.1:c.3142A>G	NP_001124451.1:p.Thr1048Ala
NM_001130980.1:c.3100A>G	NP_001124452.1:p.Thr1034Ala
NM_001130981.1:c.3100A>G	NP_001124453.1:p.Thr1034Ala
NM_001130982.1:c.3145A>G	NP_001124454.1:p.Thr1049Ala
NM_001130983.1:c.3052A>G	NP_001124455.1:p.Thr1018Ala
NM_001130984.1:c.3010A>G	NP_001124456.1:p.Thr1004Ala
NM_001130985.1:c.3103A>G	NP_001124457.1:p.Thr1035Ala
NM_001130986.1:c.3010A>G	NP_001124458.1:p.Thr1004Ala
NM_001130987.1:c.3103A>G	NP_001124459.1:p.Thr1035Ala
NM_003494.3:c.3049A>G	NP_003485.1:p.Thr1017Ala
XM_005264584.3:c.3145A>G	XP_005264641.1:p.Thr1049Ala
XM_005264585.3:c.3142A>G	XP_005264642.1:p.Thr1048Ala
XM_005264584.4:c.3145A>G	XP_005264641.1:p.Thr1049Ala
XM_005264585.5:c.3142A>G	XP_005264642.1:p.Thr1048Ala
XR_001738969.1:n.3303A>G
NM_001130987.2:c.3103A>G MANE Select	NP_001124459.1:p.Thr1035Ala
NM_001130455.2:c.3052A>G	NP_001123927.1:p.Thr1018Ala
NM_001130976.2:c.3007A>G	NP_001124448.1:p.Thr1003Ala
NM_001130977.2:c.3007A>G	NP_001124449.1:p.Thr1003Ala
NM_001130978.2:c.3049A>G	NP_001124450.1:p.Thr1017Ala
NM_001130979.2:c.3142A>G	NP_001124451.1:p.Thr1048Ala
NM_001130980.2:c.3100A>G	NP_001124452.1:p.Thr1034Ala
NM_001130981.2:c.3100A>G	NP_001124453.1:p.Thr1034Ala
NM_001130982.2:c.3145A>G	NP_001124454.1:p.Thr1049Ala
NM_001130983.2:c.3052A>G	NP_001124455.1:p.Thr1018Ala
NM_001130984.2:c.3010A>G	NP_001124456.1:p.Thr1004Ala
NM_001130985.2:c.3103A>G	NP_001124457.1:p.Thr1035Ala
NM_001130986.2:c.3010A>G	NP_001124458.1:p.Thr1004Ala
NM_003494.4:c.3049A>G MANE Plus Clinical	NP_003485.1:p.Thr1017Ala