Canonical Allele Identifier: CA2673418250

Gene: C5orf22

Linked Data

• gnomAD v4: 5-31532475-T-TTCTACCCTTTATATACC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532475_31532476insTCTACCCTTTATATACC , CM000667.2:g.31532475_31532476insTCTACCCTTTATATACC	GRCh38
NC_000005.9:g.31532582_31532583insTCTACCCTTTATATACC , CM000667.1:g.31532582_31532583insTCTACCCTTTATATACC	GRCh37
NC_000005.8:g.31568339_31568340insTCTACCCTTTATATACC	NCBI36
NG_051574.1:g.4700_4701insGGTATATAAAGGGTAGA

Transcript Alleles

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