Canonical Allele Identifier: CA1537095122

Gene: C5orf22

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532376C= , CM000667.2:g.31532376C=	GRCh38
NC_000005.9:g.31532483C= , CM000667.1:g.31532483C=	GRCh37
NC_000005.8:g.31568240C=	NCBI36
NG_051574.1:g.4800G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.-17C= MANE Select	ENSP00000326879.9:n.-17C=
ENST00000325366.13:c.-17C=	ENSP00000326879.9:n.-17C=
ENST00000504464.5:c.-17C=	ENSP00000430261.1:n.-17C=
ENST00000507818.6:c.-17C=	ENSP00000430860.1:n.-17C=
ENST00000510659.5:c.-17C=	ENSP00000423039.1:n.-17C=
ENST00000511208.2:c.-17C=	ENSP00000428898.1:n.-17C=
ENST00000513967.5:c.-17C=	ENSP00000421667.1:n.-17C=
ENST00000515409.5:n.82C=
ENST00000517780.1:n.82C=
NM_018356.2:c.-17C=	NP_060826.2:n.-17C=
XM_005248319.2:c.-588C=	XP_005248376.1:n.-588C=
XM_006714479.1:c.-177C=	XP_006714542.1:n.-177C=
XM_006714480.2:c.-499C=	XP_006714543.1:n.-499C=
XM_011514062.1:c.-17C=	XP_011512364.1:n.-17C=
NR_134298.1:n.111C=
XM_006714479.2:c.-177C=	XP_006714542.1:n.-177C=
XM_006714480.3:c.-499C=	XP_006714543.1:n.-499C=
XM_011514062.3:c.-17C=	XP_011512364.1:n.-17C=
XM_017009607.1:c.-17C=	XP_016865096.1:n.-17C=
XM_017009608.2:c.-17C=	XP_016865097.1:n.-17C=
XM_017009609.1:c.-177C=	XP_016865098.1:n.-177C=
XM_017009610.1:c.-591C=	XP_016865099.1:n.-591C=
XM_017009611.2:c.-588C=	XP_016865100.1:n.-588C=
XM_017009612.2:c.-499C=	XP_016865101.1:n.-499C=
XM_017009613.2:c.-591C=	XP_016865102.1:n.-591C=
XM_017009614.1:c.-684C=	XP_016865103.1:n.-684C=
XM_017009615.1:c.-592C=	XP_016865104.1:n.-592C=
XM_017009616.1:c.-496C=	XP_016865105.1:n.-496C=
NM_018356.3:c.-17C= MANE Select	NP_060826.2:n.-17C=
NR_134298.2:n.76C=