Canonical Allele Identifier: CA443642586

Gene: C5orf22

Linked Data

• MyVariant Identifiers: chr5:g.31532526T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532419T>C , CM000667.2:g.31532419T>C	GRCh38
NC_000005.9:g.31532526T>C , CM000667.1:g.31532526T>C	GRCh37
NC_000005.8:g.31568283T>C	NCBI36
NG_051574.1:g.4757A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.27T>C MANE Select	ENSP00000326879.9:p.Ala9=
ENST00000325366.13:c.27T>C	ENSP00000326879.9:p.Ala9=
ENST00000504464.5:c.27T>C	ENSP00000430261.1:p.Ala9=
ENST00000507818.6:c.27T>C	ENSP00000430860.1:p.Ala9=
ENST00000510659.5:c.27T>C	ENSP00000423039.1:p.Ala9=
ENST00000511208.2:c.27T>C	ENSP00000428898.1:p.Ala9=
ENST00000513967.5:c.27T>C	ENSP00000421667.1:p.Ala9=
ENST00000515409.5:n.125T>C
ENST00000517780.1:n.125T>C
NM_018356.2:c.27T>C	NP_060826.2:p.Ala9=
XM_005248319.2:c.-545T>C	XP_005248376.1:n.-545T>C
XM_006714479.1:c.-134T>C	XP_006714542.1:n.-134T>C
XM_006714480.2:c.-456T>C	XP_006714543.1:n.-456T>C
XM_011514062.1:c.27T>C	XP_011512364.1:p.Ala9=
NR_134298.1:n.154T>C
XM_006714479.2:c.-134T>C	XP_006714542.1:n.-134T>C
XM_006714480.3:c.-456T>C	XP_006714543.1:n.-456T>C
XM_011514062.3:c.27T>C	XP_011512364.1:p.Ala9=
XM_017009607.1:c.27T>C	XP_016865096.1:p.Ala9=
XM_017009608.2:c.27T>C	XP_016865097.1:p.Ala9=
XM_017009609.1:c.-134T>C	XP_016865098.1:n.-134T>C
XM_017009610.1:c.-548T>C	XP_016865099.1:n.-548T>C
XM_017009611.2:c.-545T>C	XP_016865100.1:n.-545T>C
XM_017009612.2:c.-456T>C	XP_016865101.1:n.-456T>C
XM_017009613.2:c.-548T>C	XP_016865102.1:n.-548T>C
XM_017009614.1:c.-641T>C	XP_016865103.1:n.-641T>C
XM_017009615.1:c.-549T>C	XP_016865104.1:n.-549T>C
XM_017009616.1:c.-453T>C	XP_016865105.1:n.-453T>C
NM_018356.3:c.27T>C MANE Select	NP_060826.2:p.Ala9=
NR_134298.2:n.119T>C