Canonical Allele Identifier: CA1537095130

Gene: C5orf22

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532381G= , CM000667.2:g.31532381G=	GRCh38
NC_000005.9:g.31532488G= , CM000667.1:g.31532488G=	GRCh37
NC_000005.8:g.31568245G=	NCBI36
NG_051574.1:g.4795C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.-12G= MANE Select	ENSP00000326879.9:n.-12G=
ENST00000325366.13:c.-12G=	ENSP00000326879.9:n.-12G=
ENST00000504464.5:c.-12G=	ENSP00000430261.1:n.-12G=
ENST00000507818.6:c.-12G=	ENSP00000430860.1:n.-12G=
ENST00000510659.5:c.-12G=	ENSP00000423039.1:n.-12G=
ENST00000511208.2:c.-12G=	ENSP00000428898.1:n.-12G=
ENST00000513967.5:c.-12G=	ENSP00000421667.1:n.-12G=
ENST00000515409.5:n.87G=
ENST00000517780.1:n.87G=
NM_018356.2:c.-12G=	NP_060826.2:n.-12G=
XM_005248319.2:c.-583G=	XP_005248376.1:n.-583G=
XM_006714479.1:c.-172G=	XP_006714542.1:n.-172G=
XM_006714480.2:c.-494G=	XP_006714543.1:n.-494G=
XM_011514062.1:c.-12G=	XP_011512364.1:n.-12G=
NR_134298.1:n.116G=
XM_006714479.2:c.-172G=	XP_006714542.1:n.-172G=
XM_006714480.3:c.-494G=	XP_006714543.1:n.-494G=
XM_011514062.3:c.-12G=	XP_011512364.1:n.-12G=
XM_017009607.1:c.-12G=	XP_016865096.1:n.-12G=
XM_017009608.2:c.-12G=	XP_016865097.1:n.-12G=
XM_017009609.1:c.-172G=	XP_016865098.1:n.-172G=
XM_017009610.1:c.-586G=	XP_016865099.1:n.-586G=
XM_017009611.2:c.-583G=	XP_016865100.1:n.-583G=
XM_017009612.2:c.-494G=	XP_016865101.1:n.-494G=
XM_017009613.2:c.-586G=	XP_016865102.1:n.-586G=
XM_017009614.1:c.-679G=	XP_016865103.1:n.-679G=
XM_017009615.1:c.-587G=	XP_016865104.1:n.-587G=
XM_017009616.1:c.-491G=	XP_016865105.1:n.-491G=
NM_018356.3:c.-12G= MANE Select	NP_060826.2:n.-12G=
NR_134298.2:n.81G=