Canonical Allele Identifier: CA913189520
Gene: SMN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 634945
ClinVar RCV Id: RCV000785816
dbSNP Id: rs1561499612

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70942358_70942368del , CM000667.2:g.70942358_70942368del GRCh38
NC_000005.9:g.70238185_70238195del , CM000667.1:g.70238185_70238195del GRCh37
NC_000005.8:g.70273941_70273951del NCBI36
NG_008691.1:g.22418_22428del , LRG_676:g.22418_22428del

Transcript Alleles

HGVS Amino-acid change
ENST00000380707.9:c.274_284del
ENST00000351205.8:c.274_284del
ENST00000380707.8:c.274_284del
ENST00000503079.6:c.274_284del
ENST00000506163.5:c.274_284del
ENST00000506239.6:c.274_284del
ENST00000514951.5:c.274-360_274-350del ENSP00000423298.1:n.274-360_274-350del
ENST00000625245.2:c.274_284del
NM_000344.3:c.274_284del , LRG_676t1:c.274_284del
NM_001297715.1:c.274_284del
NM_022874.2:c.274_284del
XM_011543596.1:c.274_284del
XM_011543597.1:c.274-360_274-350del XP_011541899.1:n.274-360_274-350del
XM_011543598.1:c.274-360_274-350del XP_011541900.1:n.274-360_274-350del
XM_011543598.3:c.274-360_274-350del XP_011541900.1:n.274-360_274-350del
XM_017009786.1:c.274_284del
NM_000344.4:c.274_284del