Canonical Allele Identifier: CA347205786

Gene: DYSF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71453999A>G , CM000664.2:g.71453999A>G	GRCh38
NC_000002.11:g.71681129A>G , CM000664.1:g.71681129A>G	GRCh37
NC_000002.10:g.71534637A>G	NCBI36
NG_008694.1:g.5377A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003494.4:c.1A>G MANE Plus Clinical	NP_003485.1:p.Met1Val
ENST00000258104.8:c.1A>G MANE Plus Clinical	ENSP00000258104.3:p.Met1Val
NM_001130976.1:c.1A>G	NP_001124448.1:p.Met1Val
NM_001130976.2:c.1A>G	NP_001124448.1:p.Met1Val
NM_001130977.1:c.1A>G	NP_001124449.1:p.Met1Val
NM_001130977.2:c.1A>G	NP_001124449.1:p.Met1Val
NM_001130978.1:c.1A>G	NP_001124450.1:p.Met1Val
NM_001130978.2:c.1A>G	NP_001124450.1:p.Met1Val
NM_001130979.1:c.1A>G	NP_001124451.1:p.Met1Val
NM_001130979.2:c.1A>G	NP_001124451.1:p.Met1Val
NM_001130980.1:c.1A>G	NP_001124452.1:p.Met1Val
NM_001130980.2:c.1A>G	NP_001124452.1:p.Met1Val
NM_001130981.1:c.1A>G	NP_001124453.1:p.Met1Val
NM_001130981.2:c.1A>G	NP_001124453.1:p.Met1Val
NM_003494.3:c.1A>G	NP_003485.1:p.Met1Val
ENST00000258104.7:c.1A>G	ENSP00000258104.3:p.Met1Val
ENST00000409582.7:c.1A>G	ENSP00000386547.3:p.Met1Val
ENST00000409762.5:c.1A>G	ENSP00000387137.1:p.Met1Val
ENST00000413539.6:c.1A>G	ENSP00000407046.2:p.Met1Val
ENST00000429174.6:c.1A>G	ENSP00000398305.2:p.Met1Val
XM_005264585.3:c.1A>G	XP_005264642.1:p.Met1Val
XM_005264585.5:c.1A>G	XP_005264642.1:p.Met1Val