Canonical Allele Identifier: CA2659555582

Gene: DYSF

Linked Data

• gnomAD v4: 2-71669454-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71669454G>T , CM000664.2:g.71669454G>T	GRCh38
NC_000002.11:g.71896584G>T , CM000664.1:g.71896584G>T	GRCh37
NC_000002.10:g.71750092G>T	NCBI36
NG_008694.1:g.220832G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3057-151G>T	ENSP00000513536.1:n.3057-151G>T
ENST00000698058.1:c.2274-151G>T	ENSP00000513537.1:n.2274-151G>T
ENST00000698059.1:c.2382-151G>T	ENSP00000513538.1:n.2382-151G>T
ENST00000258104.8:c.5526-151G>T MANE Plus Clinical	ENSP00000258104.3:n.5526-151G>T
ENST00000410020.8:c.5643-151G>T MANE Select	ENSP00000386881.3:n.5643-151G>T
ENST00000258104.7:c.5526-151G>T	ENSP00000258104.3:n.5526-151G>T
ENST00000394120.6:c.5529-151G>T	ENSP00000377678.2:n.5529-151G>T
ENST00000409366.5:c.5592-151G>T	ENSP00000386512.1:n.5592-151G>T
ENST00000409582.7:c.5640-151G>T	ENSP00000386547.3:n.5640-151G>T
ENST00000409651.5:c.5622-151G>T	ENSP00000386683.1:n.5622-151G>T
ENST00000409744.5:c.5550-151G>T	ENSP00000386285.1:n.5550-151G>T
ENST00000409762.5:c.5577-151G>T	ENSP00000387137.1:n.5577-151G>T
ENST00000410020.7:c.5643-151G>T	ENSP00000386881.3:n.5643-151G>T
ENST00000410041.1:c.5580-151G>T	ENSP00000386617.1:n.5580-151G>T
ENST00000413539.6:c.5619-151G>T	ENSP00000407046.2:n.5619-151G>T
ENST00000429174.6:c.5589-151G>T	ENSP00000398305.2:n.5589-151G>T
ENST00000479049.6:n.2411-151G>T
NM_001130455.1:c.5529-151G>T	NP_001123927.1:n.5529-151G>T
NM_001130976.1:c.5484-151G>T	NP_001124448.1:n.5484-151G>T
NM_001130977.1:c.5547-151G>T	NP_001124449.1:n.5547-151G>T
NM_001130978.1:c.5589-151G>T	NP_001124450.1:n.5589-151G>T
NM_001130979.1:c.5619-151G>T	NP_001124451.1:n.5619-151G>T
NM_001130980.1:c.5577-151G>T	NP_001124452.1:n.5577-151G>T
NM_001130981.1:c.5640-151G>T	NP_001124453.1:n.5640-151G>T
NM_001130982.1:c.5622-151G>T	NP_001124454.1:n.5622-151G>T
NM_001130983.1:c.5592-151G>T	NP_001124455.1:n.5592-151G>T
NM_001130984.1:c.5550-151G>T	NP_001124456.1:n.5550-151G>T
NM_001130985.1:c.5580-151G>T	NP_001124457.1:n.5580-151G>T
NM_001130986.1:c.5487-151G>T	NP_001124458.1:n.5487-151G>T
NM_001130987.1:c.5643-151G>T	NP_001124459.1:n.5643-151G>T
NM_003494.3:c.5526-151G>T	NP_003485.1:n.5526-151G>T
XM_005264584.3:c.5685-151G>T	XP_005264641.1:n.5685-151G>T
XM_005264585.3:c.5682-151G>T	XP_005264642.1:n.5682-151G>T
XM_005264584.4:c.5685-151G>T	XP_005264641.1:n.5685-151G>T
XM_005264585.5:c.5682-151G>T	XP_005264642.1:n.5682-151G>T
NM_001130987.2:c.5643-151G>T MANE Select	NP_001124459.1:n.5643-151G>T
NM_001130455.2:c.5529-151G>T	NP_001123927.1:n.5529-151G>T
NM_001130976.2:c.5484-151G>T	NP_001124448.1:n.5484-151G>T
NM_001130977.2:c.5547-151G>T	NP_001124449.1:n.5547-151G>T
NM_001130978.2:c.5589-151G>T	NP_001124450.1:n.5589-151G>T
NM_001130979.2:c.5619-151G>T	NP_001124451.1:n.5619-151G>T
NM_001130980.2:c.5577-151G>T	NP_001124452.1:n.5577-151G>T
NM_001130981.2:c.5640-151G>T	NP_001124453.1:n.5640-151G>T
NM_001130982.2:c.5622-151G>T	NP_001124454.1:n.5622-151G>T
NM_001130983.2:c.5592-151G>T	NP_001124455.1:n.5592-151G>T
NM_001130984.2:c.5550-151G>T	NP_001124456.1:n.5550-151G>T
NM_001130985.2:c.5580-151G>T	NP_001124457.1:n.5580-151G>T
NM_001130986.2:c.5487-151G>T	NP_001124458.1:n.5487-151G>T
NM_003494.4:c.5526-151G>T MANE Plus Clinical	NP_003485.1:n.5526-151G>T