Canonical Allele Identifier: CA649895198

Gene: C5orf22

Linked Data

• COSMIC: COSN16667349

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532342_31532343insA , CM000667.2:g.31532342_31532343insA	GRCh38
NC_000005.9:g.31532449_31532450insA , CM000667.1:g.31532449_31532450insA	GRCh37
NC_000005.8:g.31568206_31568207insA	NCBI36
NG_051574.1:g.4833_4834insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.-51_-50insA MANE Select	ENSP00000326879.9:n.-51_-50insA
ENST00000325366.13:c.-51_-50insA	ENSP00000326879.9:n.-51_-50insA
ENST00000504464.5:c.-51_-50insA	ENSP00000430261.1:n.-51_-50insA
ENST00000507818.6:c.-51_-50insA	ENSP00000430860.1:n.-51_-50insA
ENST00000510659.5:c.-51_-50insA	ENSP00000423039.1:n.-51_-50insA
ENST00000511208.2:c.-51_-50insA	ENSP00000428898.1:n.-51_-50insA
ENST00000513967.5:c.-51_-50insA	ENSP00000421667.1:n.-51_-50insA
ENST00000515409.5:n.48_49insA
ENST00000517780.1:n.48_49insA
NM_018356.2:c.-51_-50insA	NP_060826.2:n.-51_-50insA
XM_005248319.2:c.-622_-621insA	XP_005248376.1:n.-622_-621insA
XM_006714479.1:c.-211_-210insA	XP_006714542.1:n.-211_-210insA
XM_006714480.2:c.-533_-532insA	XP_006714543.1:n.-533_-532insA
XM_011514062.1:c.-51_-50insA	XP_011512364.1:n.-51_-50insA
NR_134298.1:n.77_78insA
XM_006714479.2:c.-211_-210insA	XP_006714542.1:n.-211_-210insA
XM_006714480.3:c.-533_-532insA	XP_006714543.1:n.-533_-532insA
XM_011514062.3:c.-51_-50insA	XP_011512364.1:n.-51_-50insA
XM_017009607.1:c.-51_-50insA	XP_016865096.1:n.-51_-50insA
XM_017009608.2:c.-51_-50insA	XP_016865097.1:n.-51_-50insA
XM_017009609.1:c.-211_-210insA	XP_016865098.1:n.-211_-210insA
XM_017009610.1:c.-625_-624insA	XP_016865099.1:n.-625_-624insA
XM_017009611.2:c.-622_-621insA	XP_016865100.1:n.-622_-621insA
XM_017009612.2:c.-533_-532insA	XP_016865101.1:n.-533_-532insA
XM_017009613.2:c.-625_-624insA	XP_016865102.1:n.-625_-624insA
XM_017009614.1:c.-718_-717insA	XP_016865103.1:n.-718_-717insA
XM_017009615.1:c.-626_-625insA	XP_016865104.1:n.-626_-625insA
XM_017009616.1:c.-530_-529insA	XP_016865105.1:n.-530_-529insA
NM_018356.3:c.-51_-50insA MANE Select	NP_060826.2:n.-51_-50insA
NR_134298.2:n.42_43insA