Canonical Allele Identifier: CA347226308

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71906234G>C (hg19) ; chr2:g.71679104G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71679104G>C , CM000664.2:g.71679104G>C	GRCh38
NC_000002.11:g.71906234G>C , CM000664.1:g.71906234G>C	GRCh37
NC_000002.10:g.71759742G>C	NCBI36
NG_008694.1:g.230482G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698057.1:c.3346G>C	ENSP00000513536.1:p.Ala1116Pro
ENST00000698058.1:c.2563G>C	ENSP00000513537.1:p.Ala855Pro
ENST00000698059.1:c.2671G>C	ENSP00000513538.1:p.Ala891Pro
ENST00000258104.8:c.5815G>C MANE Plus Clinical	ENSP00000258104.3:p.Ala1939Pro
ENST00000410020.8:c.5932G>C MANE Select	ENSP00000386881.3:p.Ala1978Pro
ENST00000258104.7:c.5815G>C	ENSP00000258104.3:p.Ala1939Pro
ENST00000394120.6:c.5818G>C	ENSP00000377678.2:p.Ala1940Pro
ENST00000409366.5:c.5881G>C	ENSP00000386512.1:p.Ala1961Pro
ENST00000409582.7:c.5929G>C	ENSP00000386547.3:p.Ala1977Pro
ENST00000409651.5:c.5911G>C	ENSP00000386683.1:p.Ala1971Pro
ENST00000409744.5:c.5839G>C	ENSP00000386285.1:p.Ala1947Pro
ENST00000409762.5:c.5866G>C	ENSP00000387137.1:p.Ala1956Pro
ENST00000410020.7:c.5932G>C	ENSP00000386881.3:p.Ala1978Pro
ENST00000410041.1:c.5869G>C	ENSP00000386617.1:p.Ala1957Pro
ENST00000413539.6:c.5908G>C	ENSP00000407046.2:p.Ala1970Pro
ENST00000429174.6:c.5878G>C	ENSP00000398305.2:p.Ala1960Pro
ENST00000479049.6:n.2700G>C
NM_001130455.1:c.5818G>C	NP_001123927.1:p.Ala1940Pro
NM_001130976.1:c.5773G>C	NP_001124448.1:p.Ala1925Pro
NM_001130977.1:c.5836G>C	NP_001124449.1:p.Ala1946Pro
NM_001130978.1:c.5878G>C	NP_001124450.1:p.Ala1960Pro
NM_001130979.1:c.5908G>C	NP_001124451.1:p.Ala1970Pro
NM_001130980.1:c.5866G>C	NP_001124452.1:p.Ala1956Pro
NM_001130981.1:c.5929G>C	NP_001124453.1:p.Ala1977Pro
NM_001130982.1:c.5911G>C	NP_001124454.1:p.Ala1971Pro
NM_001130983.1:c.5881G>C	NP_001124455.1:p.Ala1961Pro
NM_001130984.1:c.5839G>C	NP_001124456.1:p.Ala1947Pro
NM_001130985.1:c.5869G>C	NP_001124457.1:p.Ala1957Pro
NM_001130986.1:c.5776G>C	NP_001124458.1:p.Ala1926Pro
NM_001130987.1:c.5932G>C	NP_001124459.1:p.Ala1978Pro
NM_003494.3:c.5815G>C	NP_003485.1:p.Ala1939Pro
XM_005264584.3:c.5974G>C	XP_005264641.1:p.Ala1992Pro
XM_005264585.3:c.5971G>C	XP_005264642.1:p.Ala1991Pro
XM_005264584.4:c.5974G>C	XP_005264641.1:p.Ala1992Pro
XM_005264585.5:c.5971G>C	XP_005264642.1:p.Ala1991Pro
NM_001130987.2:c.5932G>C MANE Select	NP_001124459.1:p.Ala1978Pro
NM_001130455.2:c.5818G>C	NP_001123927.1:p.Ala1940Pro
NM_001130976.2:c.5773G>C	NP_001124448.1:p.Ala1925Pro
NM_001130977.2:c.5836G>C	NP_001124449.1:p.Ala1946Pro
NM_001130978.2:c.5878G>C	NP_001124450.1:p.Ala1960Pro
NM_001130979.2:c.5908G>C	NP_001124451.1:p.Ala1970Pro
NM_001130980.2:c.5866G>C	NP_001124452.1:p.Ala1956Pro
NM_001130981.2:c.5929G>C	NP_001124453.1:p.Ala1977Pro
NM_001130982.2:c.5911G>C	NP_001124454.1:p.Ala1971Pro
NM_001130983.2:c.5881G>C	NP_001124455.1:p.Ala1961Pro
NM_001130984.2:c.5839G>C	NP_001124456.1:p.Ala1947Pro
NM_001130985.2:c.5869G>C	NP_001124457.1:p.Ala1957Pro
NM_001130986.2:c.5776G>C	NP_001124458.1:p.Ala1926Pro
NM_003494.4:c.5815G>C MANE Plus Clinical	NP_003485.1:p.Ala1939Pro