Canonical Allele Identifier: CA1537095202

Gene: C5orf22

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532434C= , CM000667.2:g.31532434C=	GRCh38
NC_000005.9:g.31532541C= , CM000667.1:g.31532541C=	GRCh37
NC_000005.8:g.31568298C=	NCBI36
NG_051574.1:g.4742G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.42C= MANE Select	ENSP00000326879.9:p.Tyr14=
ENST00000325366.13:c.42C=	ENSP00000326879.9:p.Tyr14=
ENST00000504464.5:c.42C=	ENSP00000430261.1:p.Tyr14=
ENST00000507818.6:c.42C=	ENSP00000430860.1:p.Tyr14=
ENST00000510659.5:c.42C=	ENSP00000423039.1:p.Tyr14=
ENST00000511208.2:c.42C=	ENSP00000428898.1:p.Tyr14=
ENST00000513967.5:c.42C=	ENSP00000421667.1:p.Tyr14=
ENST00000515409.5:n.140C=
ENST00000517780.1:n.140C=
NM_018356.2:c.42C=	NP_060826.2:p.Tyr14=
XM_005248319.2:c.-530C=	XP_005248376.1:n.-530C=
XM_006714479.1:c.-119C=	XP_006714542.1:n.-119C=
XM_006714480.2:c.-441C=	XP_006714543.1:n.-441C=
XM_011514062.1:c.42C=	XP_011512364.1:p.Tyr14=
NR_134298.1:n.169C=
XM_006714479.2:c.-119C=	XP_006714542.1:n.-119C=
XM_006714480.3:c.-441C=	XP_006714543.1:n.-441C=
XM_011514062.3:c.42C=	XP_011512364.1:p.Tyr14=
XM_017009607.1:c.42C=	XP_016865096.1:p.Tyr14=
XM_017009608.2:c.42C=	XP_016865097.1:p.Tyr14=
XM_017009609.1:c.-119C=	XP_016865098.1:n.-119C=
XM_017009610.1:c.-533C=	XP_016865099.1:n.-533C=
XM_017009611.2:c.-530C=	XP_016865100.1:n.-530C=
XM_017009612.2:c.-441C=	XP_016865101.1:n.-441C=
XM_017009613.2:c.-533C=	XP_016865102.1:n.-533C=
XM_017009614.1:c.-626C=	XP_016865103.1:n.-626C=
XM_017009615.1:c.-534C=	XP_016865104.1:n.-534C=
XM_017009616.1:c.-438C=	XP_016865105.1:n.-438C=
NM_018356.3:c.42C= MANE Select	NP_060826.2:p.Tyr14=
NR_134298.2:n.134C=