Canonical Allele Identifier: CA347223031

Gene: DYSF

Linked Data

• gnomAD v4: 2-71669184-G-C
• MyVariant Identifiers: chr2:g.71896314G>C (hg19) ; chr2:g.71669184G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71669184G>C , CM000664.2:g.71669184G>C	GRCh38
NC_000002.11:g.71896314G>C , CM000664.1:g.71896314G>C	GRCh37
NC_000002.10:g.71749822G>C	NCBI36
NG_008694.1:g.220562G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3033G>C	ENSP00000513536.1:p.Lys1011Asn
ENST00000698058.1:c.2250G>C	ENSP00000513537.1:p.Lys750Asn
ENST00000698059.1:c.2358G>C	ENSP00000513538.1:p.Lys786Asn
ENST00000258104.8:c.5502G>C MANE Plus Clinical	ENSP00000258104.3:p.Lys1834Asn
ENST00000410020.8:c.5619G>C MANE Select	ENSP00000386881.3:p.Lys1873Asn
ENST00000258104.7:c.5502G>C	ENSP00000258104.3:p.Lys1834Asn
ENST00000394120.6:c.5505G>C	ENSP00000377678.2:p.Lys1835Asn
ENST00000409366.5:c.5568G>C	ENSP00000386512.1:p.Lys1856Asn
ENST00000409582.7:c.5616G>C	ENSP00000386547.3:p.Lys1872Asn
ENST00000409651.5:c.5598G>C	ENSP00000386683.1:p.Lys1866Asn
ENST00000409744.5:c.5526G>C	ENSP00000386285.1:p.Lys1842Asn
ENST00000409762.5:c.5553G>C	ENSP00000387137.1:p.Lys1851Asn
ENST00000410020.7:c.5619G>C	ENSP00000386881.3:p.Lys1873Asn
ENST00000410041.1:c.5556G>C	ENSP00000386617.1:p.Lys1852Asn
ENST00000413539.6:c.5595G>C	ENSP00000407046.2:p.Lys1865Asn
ENST00000429174.6:c.5565G>C	ENSP00000398305.2:p.Lys1855Asn
ENST00000479049.6:n.2387G>C
NM_001130455.1:c.5505G>C	NP_001123927.1:p.Lys1835Asn
NM_001130976.1:c.5460G>C	NP_001124448.1:p.Lys1820Asn
NM_001130977.1:c.5523G>C	NP_001124449.1:p.Lys1841Asn
NM_001130978.1:c.5565G>C	NP_001124450.1:p.Lys1855Asn
NM_001130979.1:c.5595G>C	NP_001124451.1:p.Lys1865Asn
NM_001130980.1:c.5553G>C	NP_001124452.1:p.Lys1851Asn
NM_001130981.1:c.5616G>C	NP_001124453.1:p.Lys1872Asn
NM_001130982.1:c.5598G>C	NP_001124454.1:p.Lys1866Asn
NM_001130983.1:c.5568G>C	NP_001124455.1:p.Lys1856Asn
NM_001130984.1:c.5526G>C	NP_001124456.1:p.Lys1842Asn
NM_001130985.1:c.5556G>C	NP_001124457.1:p.Lys1852Asn
NM_001130986.1:c.5463G>C	NP_001124458.1:p.Lys1821Asn
NM_001130987.1:c.5619G>C	NP_001124459.1:p.Lys1873Asn
NM_003494.3:c.5502G>C	NP_003485.1:p.Lys1834Asn
XM_005264584.3:c.5661G>C	XP_005264641.1:p.Lys1887Asn
XM_005264585.3:c.5658G>C	XP_005264642.1:p.Lys1886Asn
XM_005264584.4:c.5661G>C	XP_005264641.1:p.Lys1887Asn
XM_005264585.5:c.5658G>C	XP_005264642.1:p.Lys1886Asn
NM_001130987.2:c.5619G>C MANE Select	NP_001124459.1:p.Lys1873Asn
NM_001130455.2:c.5505G>C	NP_001123927.1:p.Lys1835Asn
NM_001130976.2:c.5460G>C	NP_001124448.1:p.Lys1820Asn
NM_001130977.2:c.5523G>C	NP_001124449.1:p.Lys1841Asn
NM_001130978.2:c.5565G>C	NP_001124450.1:p.Lys1855Asn
NM_001130979.2:c.5595G>C	NP_001124451.1:p.Lys1865Asn
NM_001130980.2:c.5553G>C	NP_001124452.1:p.Lys1851Asn
NM_001130981.2:c.5616G>C	NP_001124453.1:p.Lys1872Asn
NM_001130982.2:c.5598G>C	NP_001124454.1:p.Lys1866Asn
NM_001130983.2:c.5568G>C	NP_001124455.1:p.Lys1856Asn
NM_001130984.2:c.5526G>C	NP_001124456.1:p.Lys1842Asn
NM_001130985.2:c.5556G>C	NP_001124457.1:p.Lys1852Asn
NM_001130986.2:c.5463G>C	NP_001124458.1:p.Lys1821Asn
NM_003494.4:c.5502G>C MANE Plus Clinical	NP_003485.1:p.Lys1834Asn