Canonical Allele Identifier: CA347225521
Community Standard Title: NM_001130987.2(DYSF):c.3856G>A (p.Gly1286Arg)
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71600801G>A , CM000664.2:g.71600801G>A GRCh38
NC_000002.11:g.71827931G>A , CM000664.1:g.71827931G>A GRCh37
NC_000002.10:g.71681439G>A NCBI36
NG_008694.1:g.152179G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001130987.2:c.3856G>A MANE Select NP_001124459.1:p.Gly1286Arg
ENST00000410020.8:c.3856G>A MANE Select ENSP00000386881.3:p.Gly1286Arg
NM_003494.4:c.3802G>A MANE Plus Clinical NP_003485.1:p.Gly1268Arg
ENST00000258104.8:c.3802G>A MANE Plus Clinical ENSP00000258104.3:p.Gly1268Arg
NM_001130455.1:c.3805G>A NP_001123927.1:p.Gly1269Arg
NM_001130455.2:c.3805G>A NP_001123927.1:p.Gly1269Arg
NM_001130976.1:c.3760G>A NP_001124448.1:p.Gly1254Arg
NM_001130976.2:c.3760G>A NP_001124448.1:p.Gly1254Arg
NM_001130977.1:c.3760G>A NP_001124449.1:p.Gly1254Arg
NM_001130977.2:c.3760G>A NP_001124449.1:p.Gly1254Arg
NM_001130978.1:c.3802G>A NP_001124450.1:p.Gly1268Arg
NM_001130978.2:c.3802G>A NP_001124450.1:p.Gly1268Arg
NM_001130979.1:c.3895G>A NP_001124451.1:p.Gly1299Arg
NM_001130979.2:c.3895G>A NP_001124451.1:p.Gly1299Arg
NM_001130980.1:c.3853G>A NP_001124452.1:p.Gly1285Arg
NM_001130980.2:c.3853G>A NP_001124452.1:p.Gly1285Arg
NM_001130981.1:c.3853G>A NP_001124453.1:p.Gly1285Arg
NM_001130981.2:c.3853G>A NP_001124453.1:p.Gly1285Arg
NM_001130982.1:c.3898G>A NP_001124454.1:p.Gly1300Arg
NM_001130982.2:c.3898G>A NP_001124454.1:p.Gly1300Arg
NM_001130983.1:c.3805G>A NP_001124455.1:p.Gly1269Arg
NM_001130983.2:c.3805G>A NP_001124455.1:p.Gly1269Arg
NM_001130984.1:c.3763G>A NP_001124456.1:p.Gly1255Arg
NM_001130984.2:c.3763G>A NP_001124456.1:p.Gly1255Arg
NM_001130985.1:c.3856G>A NP_001124457.1:p.Gly1286Arg
NM_001130985.2:c.3856G>A NP_001124457.1:p.Gly1286Arg
NM_001130986.1:c.3763G>A NP_001124458.1:p.Gly1255Arg
NM_001130986.2:c.3763G>A NP_001124458.1:p.Gly1255Arg
NM_001130987.1:c.3856G>A NP_001124459.1:p.Gly1286Arg
NM_003494.3:c.3802G>A NP_003485.1:p.Gly1268Arg
ENST00000258104.7:c.3802G>A ENSP00000258104.3:p.Gly1268Arg
ENST00000394120.6:c.3805G>A ENSP00000377678.2:p.Gly1269Arg
ENST00000409366.5:c.3805G>A ENSP00000386512.1:p.Gly1269Arg
ENST00000409582.7:c.3853G>A ENSP00000386547.3:p.Gly1285Arg
ENST00000409651.5:c.3898G>A ENSP00000386683.1:p.Gly1300Arg
ENST00000409744.5:c.3763G>A ENSP00000386285.1:p.Gly1255Arg
ENST00000409762.5:c.3853G>A ENSP00000387137.1:p.Gly1285Arg
ENST00000410020.7:c.3856G>A ENSP00000386881.3:p.Gly1286Arg
ENST00000410041.1:c.3856G>A ENSP00000386617.1:p.Gly1286Arg
ENST00000413539.6:c.3895G>A ENSP00000407046.2:p.Gly1299Arg
ENST00000429174.6:c.3802G>A ENSP00000398305.2:p.Gly1268Arg
ENST00000475076.5:n.630G>A
ENST00000479049.6:n.687G>A
ENST00000493767.1:n.523G>A
ENST00000698057.1:c.1228G>A ENSP00000513536.1:p.Gly410Arg
ENST00000698058.1:c.445G>A ENSP00000513537.1:p.Gly149Arg
ENST00000698059.1:c.445G>A ENSP00000513538.1:p.Gly149Arg
XM_005264584.3:c.3898G>A XP_005264641.1:p.Gly1300Arg
XM_005264584.4:c.3898G>A XP_005264641.1:p.Gly1300Arg
XM_005264585.3:c.3895G>A XP_005264642.1:p.Gly1299Arg
XM_005264585.5:c.3895G>A XP_005264642.1:p.Gly1299Arg
XR_001738969.1:n.4056G>A