Canonical Allele Identifier: CA1537095169

Gene: C5orf22

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532406C= , CM000667.2:g.31532406C=	GRCh38
NC_000005.9:g.31532513C= , CM000667.1:g.31532513C=	GRCh37
NC_000005.8:g.31568270C=	NCBI36
NG_051574.1:g.4770G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.14C= MANE Select	ENSP00000326879.9:p.Ala5=
ENST00000325366.13:c.14C=	ENSP00000326879.9:p.Ala5=
ENST00000504464.5:c.14C=	ENSP00000430261.1:p.Ala5=
ENST00000507818.6:c.14C=	ENSP00000430860.1:p.Ala5=
ENST00000510659.5:c.14C=	ENSP00000423039.1:p.Ala5=
ENST00000511208.2:c.14C=	ENSP00000428898.1:p.Ala5=
ENST00000513967.5:c.14C=	ENSP00000421667.1:p.Ala5=
ENST00000515409.5:n.112C=
ENST00000517780.1:n.112C=
NM_018356.2:c.14C=	NP_060826.2:p.Ala5=
XM_005248319.2:c.-558C=	XP_005248376.1:n.-558C=
XM_006714479.1:c.-147C=	XP_006714542.1:n.-147C=
XM_006714480.2:c.-469C=	XP_006714543.1:n.-469C=
XM_011514062.1:c.14C=	XP_011512364.1:p.Ala5=
NR_134298.1:n.141C=
XM_006714479.2:c.-147C=	XP_006714542.1:n.-147C=
XM_006714480.3:c.-469C=	XP_006714543.1:n.-469C=
XM_011514062.3:c.14C=	XP_011512364.1:p.Ala5=
XM_017009607.1:c.14C=	XP_016865096.1:p.Ala5=
XM_017009608.2:c.14C=	XP_016865097.1:p.Ala5=
XM_017009609.1:c.-147C=	XP_016865098.1:n.-147C=
XM_017009610.1:c.-561C=	XP_016865099.1:n.-561C=
XM_017009611.2:c.-558C=	XP_016865100.1:n.-558C=
XM_017009612.2:c.-469C=	XP_016865101.1:n.-469C=
XM_017009613.2:c.-561C=	XP_016865102.1:n.-561C=
XM_017009614.1:c.-654C=	XP_016865103.1:n.-654C=
XM_017009615.1:c.-562C=	XP_016865104.1:n.-562C=
XM_017009616.1:c.-466C=	XP_016865105.1:n.-466C=
NM_018356.3:c.14C= MANE Select	NP_060826.2:p.Ala5=
NR_134298.2:n.106C=