Canonical Allele Identifier: CA244883

Gene: DYSF

Linked Data

• ClinVar Variation Id: 197005
• ClinVar RCV Id: RCV000177910 ; RCV002516759
• dbSNP Id: rs794727597
• MyVariant Identifiers: chr2:g.71838375T>C (hg19) ; chr2:g.71611245T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71611245T>C , CM000664.2:g.71611245T>C	GRCh38
NC_000002.11:g.71838375T>C , CM000664.1:g.71838375T>C	GRCh37
NC_000002.10:g.71691883T>C	NCBI36
NG_008694.1:g.162623T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.1372T>C	ENSP00000513536.1:p.Ser458Pro
ENST00000698058.1:c.589T>C	ENSP00000513537.1:p.Ser197Pro
ENST00000698059.1:c.547T>C	ENSP00000513538.1:p.Ser183Pro
ENST00000258104.8:c.3904T>C MANE Plus Clinical	ENSP00000258104.3:p.Ser1302Pro
ENST00000410020.8:c.3958T>C MANE Select	ENSP00000386881.3:p.Ser1320Pro
ENST00000258104.7:c.3904T>C	ENSP00000258104.3:p.Ser1302Pro
ENST00000394120.6:c.3907T>C	ENSP00000377678.2:p.Ser1303Pro
ENST00000409366.5:c.3907T>C	ENSP00000386512.1:p.Ser1303Pro
ENST00000409582.7:c.3955T>C	ENSP00000386547.3:p.Ser1319Pro
ENST00000409651.5:c.4000T>C	ENSP00000386683.1:p.Ser1334Pro
ENST00000409744.5:c.3865T>C	ENSP00000386285.1:p.Ser1289Pro
ENST00000409762.5:c.3955T>C	ENSP00000387137.1:p.Ser1319Pro
ENST00000410020.7:c.3958T>C	ENSP00000386881.3:p.Ser1320Pro
ENST00000410041.1:c.3958T>C	ENSP00000386617.1:p.Ser1320Pro
ENST00000413539.6:c.3997T>C	ENSP00000407046.2:p.Ser1333Pro
ENST00000429174.6:c.3904T>C	ENSP00000398305.2:p.Ser1302Pro
ENST00000468173.1:n.140T>C
ENST00000472873.5:n.288T>C
ENST00000479049.6:n.789T>C
ENST00000487180.5:n.123T>C
ENST00000494501.5:n.264T>C
NM_001130455.1:c.3907T>C	NP_001123927.1:p.Ser1303Pro
NM_001130976.1:c.3862T>C	NP_001124448.1:p.Ser1288Pro
NM_001130977.1:c.3862T>C	NP_001124449.1:p.Ser1288Pro
NM_001130978.1:c.3904T>C	NP_001124450.1:p.Ser1302Pro
NM_001130979.1:c.3997T>C	NP_001124451.1:p.Ser1333Pro
NM_001130980.1:c.3955T>C	NP_001124452.1:p.Ser1319Pro
NM_001130981.1:c.3955T>C	NP_001124453.1:p.Ser1319Pro
NM_001130982.1:c.4000T>C	NP_001124454.1:p.Ser1334Pro
NM_001130983.1:c.3907T>C	NP_001124455.1:p.Ser1303Pro
NM_001130984.1:c.3865T>C	NP_001124456.1:p.Ser1289Pro
NM_001130985.1:c.3958T>C	NP_001124457.1:p.Ser1320Pro
NM_001130986.1:c.3865T>C	NP_001124458.1:p.Ser1289Pro
NM_001130987.1:c.3958T>C	NP_001124459.1:p.Ser1320Pro
NM_003494.3:c.3904T>C	NP_003485.1:p.Ser1302Pro
XM_005264584.3:c.4000T>C	XP_005264641.1:p.Ser1334Pro
XM_005264585.3:c.3997T>C	XP_005264642.1:p.Ser1333Pro
XM_005264584.4:c.4000T>C	XP_005264641.1:p.Ser1334Pro
XM_005264585.5:c.3997T>C	XP_005264642.1:p.Ser1333Pro
XR_001738969.1:n.4158T>C
NM_001130987.2:c.3958T>C MANE Select	NP_001124459.1:p.Ser1320Pro
NM_001130455.2:c.3907T>C	NP_001123927.1:p.Ser1303Pro
NM_001130976.2:c.3862T>C	NP_001124448.1:p.Ser1288Pro
NM_001130977.2:c.3862T>C	NP_001124449.1:p.Ser1288Pro
NM_001130978.2:c.3904T>C	NP_001124450.1:p.Ser1302Pro
NM_001130979.2:c.3997T>C	NP_001124451.1:p.Ser1333Pro
NM_001130980.2:c.3955T>C	NP_001124452.1:p.Ser1319Pro
NM_001130981.2:c.3955T>C	NP_001124453.1:p.Ser1319Pro
NM_001130982.2:c.4000T>C	NP_001124454.1:p.Ser1334Pro
NM_001130983.2:c.3907T>C	NP_001124455.1:p.Ser1303Pro
NM_001130984.2:c.3865T>C	NP_001124456.1:p.Ser1289Pro
NM_001130985.2:c.3958T>C	NP_001124457.1:p.Ser1320Pro
NM_001130986.2:c.3865T>C	NP_001124458.1:p.Ser1289Pro
NM_003494.4:c.3904T>C MANE Plus Clinical	NP_003485.1:p.Ser1302Pro