Canonical Allele Identifier: CA2673418235
Gene: C5orf22 HGNC NCBI

Linked Data

gnomAD v4: 5-31532359-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.31532359A>T , CM000667.2:g.31532359A>T GRCh38
NC_000005.9:g.31532466A>T , CM000667.1:g.31532466A>T GRCh37
NC_000005.8:g.31568223A>T NCBI36
NG_051574.1:g.4817T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325366.14:c.-34A>T MANE Select ENSP00000326879.9:n.-34A>T
ENST00000325366.13:c.-34A>T ENSP00000326879.9:n.-34A>T
ENST00000504464.5:c.-34A>T ENSP00000430261.1:n.-34A>T
ENST00000507818.6:c.-34A>T ENSP00000430860.1:n.-34A>T
ENST00000510659.5:c.-34A>T ENSP00000423039.1:n.-34A>T
ENST00000511208.2:c.-34A>T ENSP00000428898.1:n.-34A>T
ENST00000513967.5:c.-34A>T ENSP00000421667.1:n.-34A>T
ENST00000515409.5:n.65A>T
ENST00000517780.1:n.65A>T
NM_018356.2:c.-34A>T NP_060826.2:n.-34A>T
XM_005248319.2:c.-605A>T XP_005248376.1:n.-605A>T
XM_006714479.1:c.-194A>T XP_006714542.1:n.-194A>T
XM_006714480.2:c.-516A>T XP_006714543.1:n.-516A>T
XM_011514062.1:c.-34A>T XP_011512364.1:n.-34A>T
NR_134298.1:n.94A>T
XM_006714479.2:c.-194A>T XP_006714542.1:n.-194A>T
XM_006714480.3:c.-516A>T XP_006714543.1:n.-516A>T
XM_011514062.3:c.-34A>T XP_011512364.1:n.-34A>T
XM_017009607.1:c.-34A>T XP_016865096.1:n.-34A>T
XM_017009608.2:c.-34A>T XP_016865097.1:n.-34A>T
XM_017009609.1:c.-194A>T XP_016865098.1:n.-194A>T
XM_017009610.1:c.-608A>T XP_016865099.1:n.-608A>T
XM_017009611.2:c.-605A>T XP_016865100.1:n.-605A>T
XM_017009612.2:c.-516A>T XP_016865101.1:n.-516A>T
XM_017009613.2:c.-608A>T XP_016865102.1:n.-608A>T
XM_017009614.1:c.-701A>T XP_016865103.1:n.-701A>T
XM_017009615.1:c.-609A>T XP_016865104.1:n.-609A>T
XM_017009616.1:c.-513A>T XP_016865105.1:n.-513A>T
NM_018356.3:c.-34A>T MANE Select NP_060826.2:n.-34A>T
NR_134298.2:n.59A>T