Canonical Allele Identifier: CA2673418331

Gene: C5orf22

Linked Data

• gnomAD v4: 5-31532578-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532578_31532579insT , CM000667.2:g.31532578_31532579insT	GRCh38
NC_000005.9:g.31532685_31532686insT , CM000667.1:g.31532685_31532686insT	GRCh37
NC_000005.8:g.31568442_31568443insT	NCBI36
NG_051574.1:g.4597_4598insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.81+105_81+106insT MANE Select	ENSP00000326879.9:n.81+105_81+106insT
ENST00000325366.13:c.81+105_81+106insT	ENSP00000326879.9:n.81+105_81+106insT
ENST00000504464.5:c.81+105_81+106insT	ENSP00000430261.1:n.81+105_81+106insT
ENST00000507818.6:c.81+105_81+106insT	ENSP00000430860.1:n.81+105_81+106insT
ENST00000510659.5:c.81+105_81+106insT	ENSP00000423039.1:n.81+105_81+106insT
ENST00000511208.2:c.81+105_81+106insT	ENSP00000428898.1:n.81+105_81+106insT
ENST00000513967.5:c.81+105_81+106insT	ENSP00000421667.1:n.81+105_81+106insT
ENST00000515409.5:n.179+105_179+106insT
ENST00000517780.1:n.179+105_179+106insT
NM_018356.2:c.81+105_81+106insT	NP_060826.2:n.81+105_81+106insT
XM_005248319.2:c.-491+105_-491+106insT	XP_005248376.1:n.-491+105_-491+106insT
XM_006714479.1:c.-80+105_-80+106insT	XP_006714542.1:n.-80+105_-80+106insT
XM_006714480.2:c.-402+105_-402+106insT	XP_006714543.1:n.-402+105_-402+106insT
XM_011514062.1:c.81+105_81+106insT	XP_011512364.1:n.81+105_81+106insT
NR_134298.1:n.208+105_208+106insT
XM_006714479.2:c.-80+105_-80+106insT	XP_006714542.1:n.-80+105_-80+106insT
XM_006714480.3:c.-402+105_-402+106insT	XP_006714543.1:n.-402+105_-402+106insT
XM_011514062.3:c.81+105_81+106insT	XP_011512364.1:n.81+105_81+106insT
XM_017009607.1:c.81+105_81+106insT	XP_016865096.1:n.81+105_81+106insT
XM_017009608.2:c.81+105_81+106insT	XP_016865097.1:n.81+105_81+106insT
XM_017009609.1:c.-80+105_-80+106insT	XP_016865098.1:n.-80+105_-80+106insT
XM_017009610.1:c.-494+105_-494+106insT	XP_016865099.1:n.-494+105_-494+106insT
XM_017009611.2:c.-491+105_-491+106insT	XP_016865100.1:n.-491+105_-491+106insT
XM_017009612.2:c.-402+105_-402+106insT	XP_016865101.1:n.-402+105_-402+106insT
XM_017009613.2:c.-494+105_-494+106insT	XP_016865102.1:n.-494+105_-494+106insT
XM_017009614.1:c.-587+105_-587+106insT	XP_016865103.1:n.-587+105_-587+106insT
XM_017009615.1:c.-495+105_-495+106insT	XP_016865104.1:n.-495+105_-495+106insT
XM_017009616.1:c.-399+105_-399+106insT	XP_016865105.1:n.-399+105_-399+106insT
NM_018356.3:c.81+105_81+106insT MANE Select	NP_060826.2:n.81+105_81+106insT
NR_134298.2:n.173+105_173+106insT