Canonical Allele Identifier: CA3218114
Gene: C5orf22 HGNC NCBI

Linked Data

dbSNP Id: rs546645613
gnomAD v2: 5-31532530-C-T
gnomAD v3: 5-31532423-C-T
gnomAD v4: 5-31532423-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.31532423C>T , CM000667.2:g.31532423C>T GRCh38
NC_000005.9:g.31532530C>T , CM000667.1:g.31532530C>T GRCh37
NC_000005.8:g.31568287C>T NCBI36
NG_051574.1:g.4753G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000325366.14:c.31C>T MANE Select ENSP00000326879.9:p.Leu11Phe
ENST00000325366.13:c.31C>T ENSP00000326879.9:p.Leu11Phe
ENST00000504464.5:c.31C>T ENSP00000430261.1:p.Leu11Phe
ENST00000507818.6:c.31C>T ENSP00000430860.1:p.Leu11Phe
ENST00000510659.5:c.31C>T ENSP00000423039.1:p.Leu11Phe
ENST00000511208.2:c.31C>T ENSP00000428898.1:p.Leu11Phe
ENST00000513967.5:c.31C>T ENSP00000421667.1:p.Leu11Phe
ENST00000515409.5:n.129C>T
ENST00000517780.1:n.129C>T
NM_018356.2:c.31C>T NP_060826.2:p.Leu11Phe
XM_005248319.2:c.-541C>T XP_005248376.1:n.-541C>T
XM_006714479.1:c.-130C>T XP_006714542.1:n.-130C>T
XM_006714480.2:c.-452C>T XP_006714543.1:n.-452C>T
XM_011514062.1:c.31C>T XP_011512364.1:p.Leu11Phe
NR_134298.1:n.158C>T
XM_006714479.2:c.-130C>T XP_006714542.1:n.-130C>T
XM_006714480.3:c.-452C>T XP_006714543.1:n.-452C>T
XM_011514062.3:c.31C>T XP_011512364.1:p.Leu11Phe
XM_017009607.1:c.31C>T XP_016865096.1:p.Leu11Phe
XM_017009608.2:c.31C>T XP_016865097.1:p.Leu11Phe
XM_017009609.1:c.-130C>T XP_016865098.1:n.-130C>T
XM_017009610.1:c.-544C>T XP_016865099.1:n.-544C>T
XM_017009611.2:c.-541C>T XP_016865100.1:n.-541C>T
XM_017009612.2:c.-452C>T XP_016865101.1:n.-452C>T
XM_017009613.2:c.-544C>T XP_016865102.1:n.-544C>T
XM_017009614.1:c.-637C>T XP_016865103.1:n.-637C>T
XM_017009615.1:c.-545C>T XP_016865104.1:n.-545C>T
XM_017009616.1:c.-449C>T XP_016865105.1:n.-449C>T
NM_018356.3:c.31C>T MANE Select NP_060826.2:p.Leu11Phe
NR_134298.2:n.123C>T