Canonical Allele Identifier: CA360086484
Gene: SMN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.70070714C>T , CM000667.2:g.70070714C>T GRCh38
NC_000005.9:g.69366541C>T , CM000667.1:g.69366541C>T GRCh37
NC_000005.8:g.69402297C>T NCBI36
NG_008728.1:g.26192C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000380743.9:c.797C>T MANE Select ENSP00000370119.4:p.Ser266Leu
ENST00000638794.1:c.797C>T ENSP00000492675.1:p.Ser266Leu
ENST00000380741.8:c.797C>T ENSP00000370117.5:p.Ser266Leu
ENST00000380742.8:c.701C>T ENSP00000370118.4:p.Ser234Leu
ENST00000380743.8:c.797C>T ENSP00000370119.4:p.Ser266Leu
ENST00000503678.5:n.720C>T
ENST00000505346.5:n.263C>T
ENST00000506734.5:c.797C>T ENSP00000424799.1:p.Ser266Leu
ENST00000507458.2:c.51C>T
ENST00000508258.1:n.172C>T
ENST00000509805.5:n.364C>T
ENST00000511812.5:c.596C>T ENSP00000424282.1:p.Ser199Leu
ENST00000514914.1:n.338C>T
ENST00000614240.4:c.701C>T ENSP00000479279.1:p.Ser234Leu
ENST00000626847.2:c.797C>T ENSP00000486152.1:p.Ser266Leu
ENST00000628696.2:c.797C>T ENSP00000486268.1:p.Ser266Leu
NM_017411.3:c.797C>T NP_059107.1:p.Ser266Leu
NM_022875.2:c.797C>T NP_075013.1:p.Ser266Leu
NM_022876.2:c.701C>T NP_075014.1:p.Ser234Leu
NM_022877.2:c.701C>T NP_075015.1:p.Ser234Leu
XM_011543599.1:c.797C>T XP_011541901.1:p.Ser266Leu
XM_011543600.1:c.596C>T XP_011541902.1:p.Ser199Leu
XM_011543601.1:c.596C>T XP_011541903.1:p.Ser199Leu
XM_011543602.1:c.500C>T XP_011541904.1:p.Ser167Leu
XM_011543603.1:c.500C>T XP_011541905.1:p.Ser167Leu
XR_948432.1:n.1054+82710C>T
XM_011543600.2:c.596C>T XP_011541902.1:p.Ser199Leu
XM_011543602.3:c.500C>T XP_011541904.1:p.Ser167Leu
XM_011543603.3:c.500C>T XP_011541905.1:p.Ser167Leu
XM_017009787.1:c.797C>T XP_016865276.1:p.Ser266Leu
NM_017411.4:c.797C>T MANE Select NP_059107.1:p.Ser266Leu
NM_022875.3:c.797C>T NP_075013.1:p.Ser266Leu