Canonical Allele Identifier: CA2578317508

Gene: C5orf22

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532349del , CM000667.2:g.31532349del	GRCh38
NC_000005.9:g.31532456del , CM000667.1:g.31532456del	GRCh37
NC_000005.8:g.31568213del	NCBI36
NG_051574.1:g.4827del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.-44del MANE Select	ENSP00000326879.9:n.-44del
ENST00000325366.13:c.-44del	ENSP00000326879.9:n.-44del
ENST00000504464.5:c.-44del	ENSP00000430261.1:n.-44del
ENST00000507818.6:c.-44del	ENSP00000430860.1:n.-44del
ENST00000510659.5:c.-44del	ENSP00000423039.1:n.-44del
ENST00000511208.2:c.-44del	ENSP00000428898.1:n.-44del
ENST00000513967.5:c.-44del	ENSP00000421667.1:n.-44del
ENST00000515409.5:n.55del
ENST00000517780.1:n.55del
NM_018356.2:c.-44del	NP_060826.2:n.-44del
XM_005248319.2:c.-615del	XP_005248376.1:n.-615del
XM_006714479.1:c.-204del	XP_006714542.1:n.-204del
XM_006714480.2:c.-526del	XP_006714543.1:n.-526del
XM_011514062.1:c.-44del	XP_011512364.1:n.-44del
NR_134298.1:n.84del
XM_006714479.2:c.-204del	XP_006714542.1:n.-204del
XM_006714480.3:c.-526del	XP_006714543.1:n.-526del
XM_011514062.3:c.-44del	XP_011512364.1:n.-44del
XM_017009607.1:c.-44del	XP_016865096.1:n.-44del
XM_017009608.2:c.-44del	XP_016865097.1:n.-44del
XM_017009609.1:c.-204del	XP_016865098.1:n.-204del
XM_017009610.1:c.-618del	XP_016865099.1:n.-618del
XM_017009611.2:c.-615del	XP_016865100.1:n.-615del
XM_017009612.2:c.-526del	XP_016865101.1:n.-526del
XM_017009613.2:c.-618del	XP_016865102.1:n.-618del
XM_017009614.1:c.-711del	XP_016865103.1:n.-711del
XM_017009615.1:c.-619del	XP_016865104.1:n.-619del
XM_017009616.1:c.-523del	XP_016865105.1:n.-523del
NM_018356.3:c.-44del MANE Select	NP_060826.2:n.-44del
NR_134298.2:n.49del