Canonical Allele Identifier: CA444972122
Gene: SMN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.70241898T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70946071T>C , CM000667.2:g.70946071T>C GRCh38
NC_000005.9:g.70241898T>C , CM000667.1:g.70241898T>C GRCh37
NC_000005.8:g.70277654T>C NCBI36
NG_008691.1:g.26131T>C , LRG_676:g.26131T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000380707.9:c.729T>C MANE Select ENSP00000370083.4:p.Ile243=
ENST00000351205.8:c.729T>C ENSP00000305857.5:p.Ile243=
ENST00000380707.8:c.729T>C ENSP00000370083.4:p.Ile243=
ENST00000503079.6:c.633T>C ENSP00000428128.1:p.Ile211=
ENST00000506163.5:c.729T>C ENSP00000424926.1:p.Ile243=
ENST00000506239.6:c.729T>C ENSP00000422679.2:p.Ile243=
ENST00000507905.6:c.423T>C ENSP00000430657.1:n.423T>C
ENST00000513228.1:n.296T>C
ENST00000514951.5:c.528T>C ENSP00000423298.1:p.Ile176=
ENST00000518504.5:n.246T>C
ENST00000625245.2:c.729T>C ENSP00000486539.1:p.Ile243=
NM_000344.3:c.729T>C , LRG_676t1:c.729T>C NP_000335.1:p.Ile243=
NM_001297715.1:c.729T>C NP_001284644.1:p.Ile243=
NM_022874.2:c.633T>C NP_075012.1:p.Ile211=
XM_011543596.1:c.729T>C XP_011541898.1:p.Ile243=
XM_011543597.1:c.528T>C XP_011541899.1:p.Ile176=
XM_011543598.1:c.432T>C XP_011541900.1:p.Ile144=
XM_011543598.3:c.432T>C XP_011541900.1:p.Ile144=
XM_017009786.1:c.633T>C XP_016865275.1:p.Ile211=
NM_000344.4:c.729T>C MANE Select NP_000335.1:p.Ile243=