Canonical Allele Identifier: CA558448133

Gene: C5orf22

Linked Data

• dbSNP Id: rs1463522145
• gnomAD v2: 5-31532464-C-A
• gnomAD v4: 5-31532357-C-A
• MyVariant Identifiers: chr5:g.31532464C>A (hg19) ; chr5:g.31532357C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532357C>A , CM000667.2:g.31532357C>A	GRCh38
NC_000005.9:g.31532464C>A , CM000667.1:g.31532464C>A	GRCh37
NC_000005.8:g.31568221C>A	NCBI36
NG_051574.1:g.4819G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.-36C>A MANE Select	ENSP00000326879.9:n.-36C>A
ENST00000325366.13:c.-36C>A	ENSP00000326879.9:n.-36C>A
ENST00000504464.5:c.-36C>A	ENSP00000430261.1:n.-36C>A
ENST00000507818.6:c.-36C>A	ENSP00000430860.1:n.-36C>A
ENST00000510659.5:c.-36C>A	ENSP00000423039.1:n.-36C>A
ENST00000511208.2:c.-36C>A	ENSP00000428898.1:n.-36C>A
ENST00000513967.5:c.-36C>A	ENSP00000421667.1:n.-36C>A
ENST00000515409.5:n.63C>A
ENST00000517780.1:n.63C>A
NM_018356.2:c.-36C>A	NP_060826.2:n.-36C>A
XM_005248319.2:c.-607C>A	XP_005248376.1:n.-607C>A
XM_006714479.1:c.-196C>A	XP_006714542.1:n.-196C>A
XM_006714480.2:c.-518C>A	XP_006714543.1:n.-518C>A
XM_011514062.1:c.-36C>A	XP_011512364.1:n.-36C>A
NR_134298.1:n.92C>A
XM_006714479.2:c.-196C>A	XP_006714542.1:n.-196C>A
XM_006714480.3:c.-518C>A	XP_006714543.1:n.-518C>A
XM_011514062.3:c.-36C>A	XP_011512364.1:n.-36C>A
XM_017009607.1:c.-36C>A	XP_016865096.1:n.-36C>A
XM_017009608.2:c.-36C>A	XP_016865097.1:n.-36C>A
XM_017009609.1:c.-196C>A	XP_016865098.1:n.-196C>A
XM_017009610.1:c.-610C>A	XP_016865099.1:n.-610C>A
XM_017009611.2:c.-607C>A	XP_016865100.1:n.-607C>A
XM_017009612.2:c.-518C>A	XP_016865101.1:n.-518C>A
XM_017009613.2:c.-610C>A	XP_016865102.1:n.-610C>A
XM_017009614.1:c.-703C>A	XP_016865103.1:n.-703C>A
XM_017009615.1:c.-611C>A	XP_016865104.1:n.-611C>A
XM_017009616.1:c.-515C>A	XP_016865105.1:n.-515C>A
NM_018356.3:c.-36C>A MANE Select	NP_060826.2:n.-36C>A
NR_134298.2:n.57C>A