Canonical Allele Identifier: CA1537095138

Gene: C5orf22

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532385G= , CM000667.2:g.31532385G=	GRCh38
NC_000005.9:g.31532492G= , CM000667.1:g.31532492G=	GRCh37
NC_000005.8:g.31568249G=	NCBI36
NG_051574.1:g.4791C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.-8G= MANE Select	ENSP00000326879.9:n.-8G=
ENST00000325366.13:c.-8G=	ENSP00000326879.9:n.-8G=
ENST00000504464.5:c.-8G=	ENSP00000430261.1:n.-8G=
ENST00000507818.6:c.-8G=	ENSP00000430860.1:n.-8G=
ENST00000510659.5:c.-8G=	ENSP00000423039.1:n.-8G=
ENST00000511208.2:c.-8G=	ENSP00000428898.1:n.-8G=
ENST00000513967.5:c.-8G=	ENSP00000421667.1:n.-8G=
ENST00000515409.5:n.91G=
ENST00000517780.1:n.91G=
NM_018356.2:c.-8G=	NP_060826.2:n.-8G=
XM_005248319.2:c.-579G=	XP_005248376.1:n.-579G=
XM_006714479.1:c.-168G=	XP_006714542.1:n.-168G=
XM_006714480.2:c.-490G=	XP_006714543.1:n.-490G=
XM_011514062.1:c.-8G=	XP_011512364.1:n.-8G=
NR_134298.1:n.120G=
XM_006714479.2:c.-168G=	XP_006714542.1:n.-168G=
XM_006714480.3:c.-490G=	XP_006714543.1:n.-490G=
XM_011514062.3:c.-8G=	XP_011512364.1:n.-8G=
XM_017009607.1:c.-8G=	XP_016865096.1:n.-8G=
XM_017009608.2:c.-8G=	XP_016865097.1:n.-8G=
XM_017009609.1:c.-168G=	XP_016865098.1:n.-168G=
XM_017009610.1:c.-582G=	XP_016865099.1:n.-582G=
XM_017009611.2:c.-579G=	XP_016865100.1:n.-579G=
XM_017009612.2:c.-490G=	XP_016865101.1:n.-490G=
XM_017009613.2:c.-582G=	XP_016865102.1:n.-582G=
XM_017009614.1:c.-675G=	XP_016865103.1:n.-675G=
XM_017009615.1:c.-583G=	XP_016865104.1:n.-583G=
XM_017009616.1:c.-487G=	XP_016865105.1:n.-487G=
NM_018356.3:c.-8G= MANE Select	NP_060826.2:n.-8G=
NR_134298.2:n.85G=