Canonical Allele Identifier: CA347228816

Gene: DYSF

Linked Data

• ClinVar Variation Id: 864337
• ClinVar RCV Id: RCV001071496
• dbSNP Id: rs2093763492
• MyVariant Identifiers: chr2:g.71838728T>C (hg19) ; chr2:g.71611598T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71611598T>C , CM000664.2:g.71611598T>C	GRCh38
NC_000002.11:g.71838728T>C , CM000664.1:g.71838728T>C	GRCh37
NC_000002.10:g.71692236T>C	NCBI36
NG_008694.1:g.162976T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.1607T>C	ENSP00000513536.1:p.Phe536Ser
ENST00000698058.1:c.824T>C	ENSP00000513537.1:p.Phe275Ser
ENST00000698059.1:c.782T>C	ENSP00000513538.1:p.Phe261Ser
ENST00000258104.8:c.4139T>C MANE Plus Clinical	ENSP00000258104.3:p.Phe1380Ser
ENST00000410020.8:c.4193T>C MANE Select	ENSP00000386881.3:p.Phe1398Ser
ENST00000258104.7:c.4139T>C	ENSP00000258104.3:p.Phe1380Ser
ENST00000394120.6:c.4142T>C	ENSP00000377678.2:p.Phe1381Ser
ENST00000409366.5:c.4142T>C	ENSP00000386512.1:p.Phe1381Ser
ENST00000409582.7:c.4190T>C	ENSP00000386547.3:p.Phe1397Ser
ENST00000409651.5:c.4235T>C	ENSP00000386683.1:p.Phe1412Ser
ENST00000409744.5:c.4100T>C	ENSP00000386285.1:p.Phe1367Ser
ENST00000409762.5:c.4190T>C	ENSP00000387137.1:p.Phe1397Ser
ENST00000410020.7:c.4193T>C	ENSP00000386881.3:p.Phe1398Ser
ENST00000410041.1:c.4193T>C	ENSP00000386617.1:p.Phe1398Ser
ENST00000413539.6:c.4232T>C	ENSP00000407046.2:p.Phe1411Ser
ENST00000429174.6:c.4139T>C	ENSP00000398305.2:p.Phe1380Ser
ENST00000468173.1:n.375T>C
ENST00000472873.5:n.523T>C
ENST00000479049.6:n.1024T>C
ENST00000487180.5:n.358T>C
ENST00000494501.5:n.437T>C
NM_001130455.1:c.4142T>C	NP_001123927.1:p.Phe1381Ser
NM_001130976.1:c.4097T>C	NP_001124448.1:p.Phe1366Ser
NM_001130977.1:c.4097T>C	NP_001124449.1:p.Phe1366Ser
NM_001130978.1:c.4139T>C	NP_001124450.1:p.Phe1380Ser
NM_001130979.1:c.4232T>C	NP_001124451.1:p.Phe1411Ser
NM_001130980.1:c.4190T>C	NP_001124452.1:p.Phe1397Ser
NM_001130981.1:c.4190T>C	NP_001124453.1:p.Phe1397Ser
NM_001130982.1:c.4235T>C	NP_001124454.1:p.Phe1412Ser
NM_001130983.1:c.4142T>C	NP_001124455.1:p.Phe1381Ser
NM_001130984.1:c.4100T>C	NP_001124456.1:p.Phe1367Ser
NM_001130985.1:c.4193T>C	NP_001124457.1:p.Phe1398Ser
NM_001130986.1:c.4100T>C	NP_001124458.1:p.Phe1367Ser
NM_001130987.1:c.4193T>C	NP_001124459.1:p.Phe1398Ser
NM_003494.3:c.4139T>C	NP_003485.1:p.Phe1380Ser
XM_005264584.3:c.4235T>C	XP_005264641.1:p.Phe1412Ser
XM_005264585.3:c.4232T>C	XP_005264642.1:p.Phe1411Ser
XM_005264584.4:c.4235T>C	XP_005264641.1:p.Phe1412Ser
XM_005264585.5:c.4232T>C	XP_005264642.1:p.Phe1411Ser
XR_001738969.1:n.4393T>C
NM_001130987.2:c.4193T>C MANE Select	NP_001124459.1:p.Phe1398Ser
NM_001130455.2:c.4142T>C	NP_001123927.1:p.Phe1381Ser
NM_001130976.2:c.4097T>C	NP_001124448.1:p.Phe1366Ser
NM_001130977.2:c.4097T>C	NP_001124449.1:p.Phe1366Ser
NM_001130978.2:c.4139T>C	NP_001124450.1:p.Phe1380Ser
NM_001130979.2:c.4232T>C	NP_001124451.1:p.Phe1411Ser
NM_001130980.2:c.4190T>C	NP_001124452.1:p.Phe1397Ser
NM_001130981.2:c.4190T>C	NP_001124453.1:p.Phe1397Ser
NM_001130982.2:c.4235T>C	NP_001124454.1:p.Phe1412Ser
NM_001130983.2:c.4142T>C	NP_001124455.1:p.Phe1381Ser
NM_001130984.2:c.4100T>C	NP_001124456.1:p.Phe1367Ser
NM_001130985.2:c.4193T>C	NP_001124457.1:p.Phe1398Ser
NM_001130986.2:c.4100T>C	NP_001124458.1:p.Phe1367Ser
NM_003494.4:c.4139T>C MANE Plus Clinical	NP_003485.1:p.Phe1380Ser