Canonical Allele Identifier: CA2507257528

Gene: C5orf22

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532344_31532345insTTG , CM000667.2:g.31532344_31532345insTTG	GRCh38
NC_000005.9:g.31532451_31532452insTTG , CM000667.1:g.31532451_31532452insTTG	GRCh37
NC_000005.8:g.31568208_31568209insTTG	NCBI36
NG_051574.1:g.4831_4832insCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.-49_-48insTTG MANE Select	ENSP00000326879.9:n.-49_-48insTTG
ENST00000325366.13:c.-49_-48insTTG	ENSP00000326879.9:n.-49_-48insTTG
ENST00000504464.5:c.-49_-48insTTG	ENSP00000430261.1:n.-49_-48insTTG
ENST00000507818.6:c.-49_-48insTTG	ENSP00000430860.1:n.-49_-48insTTG
ENST00000510659.5:c.-49_-48insTTG	ENSP00000423039.1:n.-49_-48insTTG
ENST00000511208.2:c.-49_-48insTTG	ENSP00000428898.1:n.-49_-48insTTG
ENST00000513967.5:c.-49_-48insTTG	ENSP00000421667.1:n.-49_-48insTTG
ENST00000515409.5:n.50_51insTTG
ENST00000517780.1:n.50_51insTTG
NM_018356.2:c.-49_-48insTTG	NP_060826.2:n.-49_-48insTTG
XM_005248319.2:c.-620_-619insTTG	XP_005248376.1:n.-620_-619insTTG
XM_006714479.1:c.-209_-208insTTG	XP_006714542.1:n.-209_-208insTTG
XM_006714480.2:c.-531_-530insTTG	XP_006714543.1:n.-531_-530insTTG
XM_011514062.1:c.-49_-48insTTG	XP_011512364.1:n.-49_-48insTTG
NR_134298.1:n.79_80insTTG
XM_006714479.2:c.-209_-208insTTG	XP_006714542.1:n.-209_-208insTTG
XM_006714480.3:c.-531_-530insTTG	XP_006714543.1:n.-531_-530insTTG
XM_011514062.3:c.-49_-48insTTG	XP_011512364.1:n.-49_-48insTTG
XM_017009607.1:c.-49_-48insTTG	XP_016865096.1:n.-49_-48insTTG
XM_017009608.2:c.-49_-48insTTG	XP_016865097.1:n.-49_-48insTTG
XM_017009609.1:c.-209_-208insTTG	XP_016865098.1:n.-209_-208insTTG
XM_017009610.1:c.-623_-622insTTG	XP_016865099.1:n.-623_-622insTTG
XM_017009611.2:c.-620_-619insTTG	XP_016865100.1:n.-620_-619insTTG
XM_017009612.2:c.-531_-530insTTG	XP_016865101.1:n.-531_-530insTTG
XM_017009613.2:c.-623_-622insTTG	XP_016865102.1:n.-623_-622insTTG
XM_017009614.1:c.-716_-715insTTG	XP_016865103.1:n.-716_-715insTTG
XM_017009615.1:c.-624_-623insTTG	XP_016865104.1:n.-624_-623insTTG
XM_017009616.1:c.-528_-527insTTG	XP_016865105.1:n.-528_-527insTTG
NM_018356.3:c.-49_-48insTTG MANE Select	NP_060826.2:n.-49_-48insTTG
NR_134298.2:n.44_45insTTG