Canonical Allele Identifier: CA3218096

Gene: C5orf22

Linked Data

• dbSNP Id: rs768434535
• ExAC: 5:31532468 C / A
• gnomAD v2: 5-31532468-C-A
• gnomAD v4: 5-31532361-C-A
• MyVariant Identifiers: chr5:g.31532468C>A (hg19) ; chr5:g.31532361C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532361C>A , CM000667.2:g.31532361C>A	GRCh38
NC_000005.9:g.31532468C>A , CM000667.1:g.31532468C>A	GRCh37
NC_000005.8:g.31568225C>A	NCBI36
NG_051574.1:g.4815G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.-32C>A MANE Select	ENSP00000326879.9:n.-32C>A
ENST00000325366.13:c.-32C>A	ENSP00000326879.9:n.-32C>A
ENST00000504464.5:c.-32C>A	ENSP00000430261.1:n.-32C>A
ENST00000507818.6:c.-32C>A	ENSP00000430860.1:n.-32C>A
ENST00000510659.5:c.-32C>A	ENSP00000423039.1:n.-32C>A
ENST00000511208.2:c.-32C>A	ENSP00000428898.1:n.-32C>A
ENST00000513967.5:c.-32C>A	ENSP00000421667.1:n.-32C>A
ENST00000515409.5:n.67C>A
ENST00000517780.1:n.67C>A
NM_018356.2:c.-32C>A	NP_060826.2:n.-32C>A
XM_005248319.2:c.-603C>A	XP_005248376.1:n.-603C>A
XM_006714479.1:c.-192C>A	XP_006714542.1:n.-192C>A
XM_006714480.2:c.-514C>A	XP_006714543.1:n.-514C>A
XM_011514062.1:c.-32C>A	XP_011512364.1:n.-32C>A
NR_134298.1:n.96C>A
XM_006714479.2:c.-192C>A	XP_006714542.1:n.-192C>A
XM_006714480.3:c.-514C>A	XP_006714543.1:n.-514C>A
XM_011514062.3:c.-32C>A	XP_011512364.1:n.-32C>A
XM_017009607.1:c.-32C>A	XP_016865096.1:n.-32C>A
XM_017009608.2:c.-32C>A	XP_016865097.1:n.-32C>A
XM_017009609.1:c.-192C>A	XP_016865098.1:n.-192C>A
XM_017009610.1:c.-606C>A	XP_016865099.1:n.-606C>A
XM_017009611.2:c.-603C>A	XP_016865100.1:n.-603C>A
XM_017009612.2:c.-514C>A	XP_016865101.1:n.-514C>A
XM_017009613.2:c.-606C>A	XP_016865102.1:n.-606C>A
XM_017009614.1:c.-699C>A	XP_016865103.1:n.-699C>A
XM_017009615.1:c.-607C>A	XP_016865104.1:n.-607C>A
XM_017009616.1:c.-511C>A	XP_016865105.1:n.-511C>A
NM_018356.3:c.-32C>A MANE Select	NP_060826.2:n.-32C>A
NR_134298.2:n.61C>A