Canonical Allele Identifier: CA347217000

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71797782C>A (hg19) ; chr2:g.71570652C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71570652C>A , CM000664.2:g.71570652C>A	GRCh38
NC_000002.11:g.71797782C>A , CM000664.1:g.71797782C>A	GRCh37
NC_000002.10:g.71651290C>A	NCBI36
NG_008694.1:g.122030C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.511C>A	ENSP00000513536.1:p.Pro171Thr
ENST00000258104.8:c.3085C>A MANE Plus Clinical	ENSP00000258104.3:p.Pro1029Thr
ENST00000410020.8:c.3139C>A MANE Select	ENSP00000386881.3:p.Pro1047Thr
ENST00000258104.7:c.3085C>A	ENSP00000258104.3:p.Pro1029Thr
ENST00000394120.6:c.3088C>A	ENSP00000377678.2:p.Pro1030Thr
ENST00000409366.5:c.3088C>A	ENSP00000386512.1:p.Pro1030Thr
ENST00000409582.7:c.3136C>A	ENSP00000386547.3:p.Pro1046Thr
ENST00000409651.5:c.3181C>A	ENSP00000386683.1:p.Pro1061Thr
ENST00000409744.5:c.3046C>A	ENSP00000386285.1:p.Pro1016Thr
ENST00000409762.5:c.3136C>A	ENSP00000387137.1:p.Pro1046Thr
ENST00000410020.7:c.3139C>A	ENSP00000386881.3:p.Pro1047Thr
ENST00000410041.1:c.3139C>A	ENSP00000386617.1:p.Pro1047Thr
ENST00000413539.6:c.3178C>A	ENSP00000407046.2:p.Pro1060Thr
ENST00000429174.6:c.3085C>A	ENSP00000398305.2:p.Pro1029Thr
ENST00000461565.1:n.251C>A
NM_001130455.1:c.3088C>A	NP_001123927.1:p.Pro1030Thr
NM_001130976.1:c.3043C>A	NP_001124448.1:p.Pro1015Thr
NM_001130977.1:c.3043C>A	NP_001124449.1:p.Pro1015Thr
NM_001130978.1:c.3085C>A	NP_001124450.1:p.Pro1029Thr
NM_001130979.1:c.3178C>A	NP_001124451.1:p.Pro1060Thr
NM_001130980.1:c.3136C>A	NP_001124452.1:p.Pro1046Thr
NM_001130981.1:c.3136C>A	NP_001124453.1:p.Pro1046Thr
NM_001130982.1:c.3181C>A	NP_001124454.1:p.Pro1061Thr
NM_001130983.1:c.3088C>A	NP_001124455.1:p.Pro1030Thr
NM_001130984.1:c.3046C>A	NP_001124456.1:p.Pro1016Thr
NM_001130985.1:c.3139C>A	NP_001124457.1:p.Pro1047Thr
NM_001130986.1:c.3046C>A	NP_001124458.1:p.Pro1016Thr
NM_001130987.1:c.3139C>A	NP_001124459.1:p.Pro1047Thr
NM_003494.3:c.3085C>A	NP_003485.1:p.Pro1029Thr
XM_005264584.3:c.3181C>A	XP_005264641.1:p.Pro1061Thr
XM_005264585.3:c.3178C>A	XP_005264642.1:p.Pro1060Thr
XM_005264584.4:c.3181C>A	XP_005264641.1:p.Pro1061Thr
XM_005264585.5:c.3178C>A	XP_005264642.1:p.Pro1060Thr
XR_001738969.1:n.3339C>A
NM_001130987.2:c.3139C>A MANE Select	NP_001124459.1:p.Pro1047Thr
NM_001130455.2:c.3088C>A	NP_001123927.1:p.Pro1030Thr
NM_001130976.2:c.3043C>A	NP_001124448.1:p.Pro1015Thr
NM_001130977.2:c.3043C>A	NP_001124449.1:p.Pro1015Thr
NM_001130978.2:c.3085C>A	NP_001124450.1:p.Pro1029Thr
NM_001130979.2:c.3178C>A	NP_001124451.1:p.Pro1060Thr
NM_001130980.2:c.3136C>A	NP_001124452.1:p.Pro1046Thr
NM_001130981.2:c.3136C>A	NP_001124453.1:p.Pro1046Thr
NM_001130982.2:c.3181C>A	NP_001124454.1:p.Pro1061Thr
NM_001130983.2:c.3088C>A	NP_001124455.1:p.Pro1030Thr
NM_001130984.2:c.3046C>A	NP_001124456.1:p.Pro1016Thr
NM_001130985.2:c.3139C>A	NP_001124457.1:p.Pro1047Thr
NM_001130986.2:c.3046C>A	NP_001124458.1:p.Pro1016Thr
NM_003494.4:c.3085C>A MANE Plus Clinical	NP_003485.1:p.Pro1029Thr