Canonical Allele Identifier: CA360097112

Gene: SMN1

Linked Data

• MyVariant Identifiers: chr5:g.70241971T>C (hg19) ; chr5:g.70946144T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.70946144T>C , CM000667.2:g.70946144T>C	GRCh38
NC_000005.9:g.70241971T>C , CM000667.1:g.70241971T>C	GRCh37
NC_000005.8:g.70277727T>C	NCBI36
NG_008691.1:g.26204T>C , LRG_676:g.26204T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380707.9:c.802T>C MANE Select	ENSP00000370083.4:p.Tyr268His
ENST00000351205.8:c.802T>C	ENSP00000305857.5:p.Tyr268His
ENST00000380707.8:c.802T>C	ENSP00000370083.4:p.Tyr268His
ENST00000503079.6:c.706T>C	ENSP00000428128.1:p.Tyr236His
ENST00000506163.5:c.802T>C	ENSP00000424926.1:p.Tyr268His
ENST00000506239.6:c.802T>C	ENSP00000422679.2:p.Tyr268His
ENST00000510679.1:n.56T>C
ENST00000513228.1:n.369T>C
ENST00000514951.5:c.601T>C	ENSP00000423298.1:p.Tyr201His
ENST00000518504.5:n.319T>C
ENST00000625245.2:c.802T>C	ENSP00000486539.1:p.Tyr268His
NM_000344.3:c.802T>C , LRG_676t1:c.802T>C	NP_000335.1:p.Tyr268His
NM_001297715.1:c.802T>C	NP_001284644.1:p.Tyr268His
NM_022874.2:c.706T>C	NP_075012.1:p.Tyr236His
XM_011543596.1:c.802T>C	XP_011541898.1:p.Tyr268His
XM_011543597.1:c.601T>C	XP_011541899.1:p.Tyr201His
XM_011543598.1:c.505T>C	XP_011541900.1:p.Tyr169His
XM_011543598.3:c.505T>C	XP_011541900.1:p.Tyr169His
XM_017009786.1:c.706T>C	XP_016865275.1:p.Tyr236His
NM_000344.4:c.802T>C MANE Select	NP_000335.1:p.Tyr268His