Canonical Allele Identifier: CA360888043

Gene: SNX24

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122999921T>G , CM000667.2:g.122999921T>G	GRCh38
NC_000005.9:g.122335616T>G , CM000667.1:g.122335616T>G	GRCh37
NC_000005.8:g.122363515T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014035.4:c.259T>G MANE Select	NP_054754.1:p.Leu87Val
ENST00000261369.9:c.259T>G MANE Select	ENSP00000261369.4:p.Leu87Val
NM_014035.2:c.259T>G	NP_054754.1:p.Leu87Val
NM_014035.3:c.259T>G	NP_054754.1:p.Leu87Val
NR_146145.1:n.574T>G
NR_146145.2:n.410T>G
ENST00000261369.8:c.259T>G	ENSP00000261369.4:p.Leu87Val
ENST00000395451.8:c.358T>G	ENSP00000378837.4:p.Leu120Val
ENST00000502387.5:n.200T>G
ENST00000503149.5:c.278T>G	ENSP00000425919.1:n.278T>G
ENST00000506996.5:c.259T>G	ENSP00000422535.1:p.Leu87Val
ENST00000507364.5:n.61T>G
ENST00000510914.5:n.115T>G
ENST00000511211.5:n.503T>G
ENST00000511545.5:c.324T>G
ENST00000513881.5:c.259T>G	ENSP00000424149.1:p.Leu87Val
ENST00000515729.1:n.79T>G
XM_005271972.3:c.259T>G	XP_005272029.1:p.Leu87Val
XM_005271972.5:c.259T>G	XP_005272029.1:p.Leu87Val
XM_006714592.2:c.259T>G	XP_006714655.1:p.Leu87Val
XM_006714592.4:c.259T>G	XP_006714655.1:p.Leu87Val
XM_011543349.1:c.358T>G	XP_011541651.1:p.Leu120Val
XM_011543349.3:c.358T>G	XP_011541651.1:p.Leu120Val
XM_011543350.1:c.358T>G	XP_011541652.1:p.Leu120Val
XM_011543350.3:c.358T>G	XP_011541652.1:p.Leu120Val
XM_011543351.1:c.358T>G	XP_011541653.1:p.Leu120Val
XM_011543352.1:c.*55T>G	XP_011541654.1:n.*55T>G
XM_017009394.1:c.178T>G	XP_016864883.1:p.Leu60Val
XM_017009395.1:c.349-29317T>G	XP_016864884.1:n.349-29317T>G
XR_001742058.1:n.578T>G