Canonical Allele Identifier: CA1537095125

Gene: C5orf22

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532379A= , CM000667.2:g.31532379A=	GRCh38
NC_000005.9:g.31532486A= , CM000667.1:g.31532486A=	GRCh37
NC_000005.8:g.31568243A=	NCBI36
NG_051574.1:g.4797T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.-14A= MANE Select	ENSP00000326879.9:n.-14A=
ENST00000325366.13:c.-14A=	ENSP00000326879.9:n.-14A=
ENST00000504464.5:c.-14A=	ENSP00000430261.1:n.-14A=
ENST00000507818.6:c.-14A=	ENSP00000430860.1:n.-14A=
ENST00000510659.5:c.-14A=	ENSP00000423039.1:n.-14A=
ENST00000511208.2:c.-14A=	ENSP00000428898.1:n.-14A=
ENST00000513967.5:c.-14A=	ENSP00000421667.1:n.-14A=
ENST00000515409.5:n.85A=
ENST00000517780.1:n.85A=
NM_018356.2:c.-14A=	NP_060826.2:n.-14A=
XM_005248319.2:c.-585A=	XP_005248376.1:n.-585A=
XM_006714479.1:c.-174A=	XP_006714542.1:n.-174A=
XM_006714480.2:c.-496A=	XP_006714543.1:n.-496A=
XM_011514062.1:c.-14A=	XP_011512364.1:n.-14A=
NR_134298.1:n.114A=
XM_006714479.2:c.-174A=	XP_006714542.1:n.-174A=
XM_006714480.3:c.-496A=	XP_006714543.1:n.-496A=
XM_011514062.3:c.-14A=	XP_011512364.1:n.-14A=
XM_017009607.1:c.-14A=	XP_016865096.1:n.-14A=
XM_017009608.2:c.-14A=	XP_016865097.1:n.-14A=
XM_017009609.1:c.-174A=	XP_016865098.1:n.-174A=
XM_017009610.1:c.-588A=	XP_016865099.1:n.-588A=
XM_017009611.2:c.-585A=	XP_016865100.1:n.-585A=
XM_017009612.2:c.-496A=	XP_016865101.1:n.-496A=
XM_017009613.2:c.-588A=	XP_016865102.1:n.-588A=
XM_017009614.1:c.-681A=	XP_016865103.1:n.-681A=
XM_017009615.1:c.-589A=	XP_016865104.1:n.-589A=
XM_017009616.1:c.-493A=	XP_016865105.1:n.-493A=
NM_018356.3:c.-14A= MANE Select	NP_060826.2:n.-14A=
NR_134298.2:n.79A=