Canonical Allele Identifier: CA2578317506

Gene: C5orf22

Linked Data

• gnomAD v4: 5-31532337-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532340del , CM000667.2:g.31532340del	GRCh38
NC_000005.9:g.31532447del , CM000667.1:g.31532447del	GRCh37
NC_000005.8:g.31568204del	NCBI36
NG_051574.1:g.4838del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.-53del MANE Select	ENSP00000326879.9:n.-53del
ENST00000325366.13:c.-53del	ENSP00000326879.9:n.-53del
ENST00000504464.5:c.-53del	ENSP00000430261.1:n.-53del
ENST00000507818.6:c.-53del	ENSP00000430860.1:n.-53del
ENST00000510659.5:c.-53del	ENSP00000423039.1:n.-53del
ENST00000511208.2:c.-53del	ENSP00000428898.1:n.-53del
ENST00000513967.5:c.-53del	ENSP00000421667.1:n.-53del
ENST00000515409.5:n.46del
ENST00000517780.1:n.46del
NM_018356.2:c.-53del	NP_060826.2:n.-53del
XM_005248319.2:c.-624del	XP_005248376.1:n.-624del
XM_006714479.1:c.-213del	XP_006714542.1:n.-213del
XM_006714480.2:c.-535del	XP_006714543.1:n.-535del
XM_011514062.1:c.-53del	XP_011512364.1:n.-53del
NR_134298.1:n.75del
XM_006714479.2:c.-213del	XP_006714542.1:n.-213del
XM_006714480.3:c.-535del	XP_006714543.1:n.-535del
XM_011514062.3:c.-53del	XP_011512364.1:n.-53del
XM_017009607.1:c.-53del	XP_016865096.1:n.-53del
XM_017009608.2:c.-53del	XP_016865097.1:n.-53del
XM_017009609.1:c.-213del	XP_016865098.1:n.-213del
XM_017009610.1:c.-627del	XP_016865099.1:n.-627del
XM_017009611.2:c.-624del	XP_016865100.1:n.-624del
XM_017009612.2:c.-535del	XP_016865101.1:n.-535del
XM_017009613.2:c.-627del	XP_016865102.1:n.-627del
XM_017009614.1:c.-720del	XP_016865103.1:n.-720del
XM_017009615.1:c.-628del	XP_016865104.1:n.-628del
XM_017009616.1:c.-532del	XP_016865105.1:n.-532del
NM_018356.3:c.-53del MANE Select	NP_060826.2:n.-53del
NR_134298.2:n.40del