Canonical Allele Identifier: CA125964867
Gene: SNX24 HGNC NCBI

Linked Data

dbSNP Id: rs2447820

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122929041G>T , CM000667.2:g.122929041G>T GRCh38
NC_000005.9:g.122264736G>T , CM000667.1:g.122264736G>T GRCh37
NC_000005.8:g.122292635G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261369.9:c.61-7693G>T MANE Select ENSP00000261369.4:n.61-7693G>T
ENST00000261369.8:c.61-7693G>T ENSP00000261369.4:n.61-7693G>T
ENST00000395451.8:c.160-7693G>T ENSP00000378837.4:n.160-7693G>T
ENST00000506996.5:c.61-7693G>T ENSP00000422535.1:n.61-7693G>T
ENST00000511211.5:n.305-7693G>T
ENST00000511545.5:c.126-7693G>T
ENST00000513613.5:n.178-7693G>T
ENST00000513881.5:c.61-7693G>T ENSP00000424149.1:n.61-7693G>T
NM_014035.2:c.61-7693G>T NP_054754.1:n.61-7693G>T
XM_005271972.3:c.61-7693G>T XP_005272029.1:n.61-7693G>T
XM_006714592.2:c.61-7693G>T XP_006714655.1:n.61-7693G>T
XM_011543349.1:c.160-7693G>T XP_011541651.1:n.160-7693G>T
XM_011543350.1:c.160-7693G>T XP_011541652.1:n.160-7693G>T
XM_011543351.1:c.160-7693G>T XP_011541653.1:n.160-7693G>T
XM_011543352.1:c.160-7693G>T XP_011541654.1:n.160-7693G>T
NM_014035.3:c.61-7693G>T NP_054754.1:n.61-7693G>T
NR_146145.1:n.246-7693G>T
XM_005271972.5:c.61-7693G>T XP_005272029.1:n.61-7693G>T
XM_006714592.4:c.61-7693G>T XP_006714655.1:n.61-7693G>T
XM_011543349.3:c.160-7693G>T XP_011541651.1:n.160-7693G>T
XM_011543350.3:c.160-7693G>T XP_011541652.1:n.160-7693G>T
XM_017009395.1:c.160-7693G>T XP_016864884.1:n.160-7693G>T
XM_017009396.1:c.160-7693G>T XP_016864885.1:n.160-7693G>T
XR_001742058.1:n.250-7693G>T
NM_014035.4:c.61-7693G>T MANE Select NP_054754.1:n.61-7693G>T
NR_146145.2:n.82-7693G>T