Canonical Allele Identifier: CA2765772348

Gene: C5orf22

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532721_31532722insCTT , CM000667.2:g.31532721_31532722insCTT	GRCh38
NC_000005.9:g.31532828_31532829insCTT , CM000667.1:g.31532828_31532829insCTT	GRCh37
NC_000005.8:g.31568585_31568586insCTT	NCBI36
NG_051574.1:g.4454_4455insAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.81+248_81+249insCTT MANE Select	ENSP00000326879.9:n.81+248_81+249insCTT
ENST00000325366.13:c.81+248_81+249insCTT	ENSP00000326879.9:n.81+248_81+249insCTT
ENST00000504464.5:c.81+248_81+249insCTT	ENSP00000430261.1:n.81+248_81+249insCTT
ENST00000507818.6:c.81+248_81+249insCTT	ENSP00000430860.1:n.81+248_81+249insCTT
ENST00000510659.5:c.81+248_81+249insCTT	ENSP00000423039.1:n.81+248_81+249insCTT
ENST00000511208.2:c.81+248_81+249insCTT	ENSP00000428898.1:n.81+248_81+249insCTT
ENST00000513967.5:c.81+248_81+249insCTT	ENSP00000421667.1:n.81+248_81+249insCTT
ENST00000515409.5:n.179+248_179+249insCTT
ENST00000517780.1:n.179+248_179+249insCTT
NM_018356.2:c.81+248_81+249insCTT	NP_060826.2:n.81+248_81+249insCTT
XM_005248319.2:c.-491+248_-491+249insCTT	XP_005248376.1:n.-491+248_-491+249insCTT
XM_006714479.1:c.-80+248_-80+249insCTT	XP_006714542.1:n.-80+248_-80+249insCTT
XM_006714480.2:c.-402+248_-402+249insCTT	XP_006714543.1:n.-402+248_-402+249insCTT
XM_011514062.1:c.81+248_81+249insCTT	XP_011512364.1:n.81+248_81+249insCTT
NR_134298.1:n.208+248_208+249insCTT
XM_006714479.2:c.-80+248_-80+249insCTT	XP_006714542.1:n.-80+248_-80+249insCTT
XM_006714480.3:c.-402+248_-402+249insCTT	XP_006714543.1:n.-402+248_-402+249insCTT
XM_011514062.3:c.81+248_81+249insCTT	XP_011512364.1:n.81+248_81+249insCTT
XM_017009607.1:c.81+248_81+249insCTT	XP_016865096.1:n.81+248_81+249insCTT
XM_017009608.2:c.81+248_81+249insCTT	XP_016865097.1:n.81+248_81+249insCTT
XM_017009609.1:c.-80+248_-80+249insCTT	XP_016865098.1:n.-80+248_-80+249insCTT
XM_017009610.1:c.-494+248_-494+249insCTT	XP_016865099.1:n.-494+248_-494+249insCTT
XM_017009611.2:c.-491+248_-491+249insCTT	XP_016865100.1:n.-491+248_-491+249insCTT
XM_017009612.2:c.-402+248_-402+249insCTT	XP_016865101.1:n.-402+248_-402+249insCTT
XM_017009613.2:c.-494+248_-494+249insCTT	XP_016865102.1:n.-494+248_-494+249insCTT
XM_017009614.1:c.-587+248_-587+249insCTT	XP_016865103.1:n.-587+248_-587+249insCTT
XM_017009615.1:c.-495+248_-495+249insCTT	XP_016865104.1:n.-495+248_-495+249insCTT
XM_017009616.1:c.-399+248_-399+249insCTT	XP_016865105.1:n.-399+248_-399+249insCTT
NM_018356.3:c.81+248_81+249insCTT MANE Select	NP_060826.2:n.81+248_81+249insCTT
NR_134298.2:n.173+248_173+249insCTT