Canonical Allele Identifier: CA359331321

Gene: C5orf22

Linked Data

• gnomAD v4: 5-31532411-G-T
• MyVariant Identifiers: chr5:g.31532518G>T (hg19) ; chr5:g.31532411G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532411G>T , CM000667.2:g.31532411G>T	GRCh38
NC_000005.9:g.31532518G>T , CM000667.1:g.31532518G>T	GRCh37
NC_000005.8:g.31568275G>T	NCBI36
NG_051574.1:g.4765C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.19G>T MANE Select	ENSP00000326879.9:p.Gly7Trp
ENST00000325366.13:c.19G>T	ENSP00000326879.9:p.Gly7Trp
ENST00000504464.5:c.19G>T	ENSP00000430261.1:p.Gly7Trp
ENST00000507818.6:c.19G>T	ENSP00000430860.1:p.Gly7Trp
ENST00000510659.5:c.19G>T	ENSP00000423039.1:p.Gly7Trp
ENST00000511208.2:c.19G>T	ENSP00000428898.1:p.Gly7Trp
ENST00000513967.5:c.19G>T	ENSP00000421667.1:p.Gly7Trp
ENST00000515409.5:n.117G>T
ENST00000517780.1:n.117G>T
NM_018356.2:c.19G>T	NP_060826.2:p.Gly7Trp
XM_005248319.2:c.-553G>T	XP_005248376.1:n.-553G>T
XM_006714479.1:c.-142G>T	XP_006714542.1:n.-142G>T
XM_006714480.2:c.-464G>T	XP_006714543.1:n.-464G>T
XM_011514062.1:c.19G>T	XP_011512364.1:p.Gly7Trp
NR_134298.1:n.146G>T
XM_006714479.2:c.-142G>T	XP_006714542.1:n.-142G>T
XM_006714480.3:c.-464G>T	XP_006714543.1:n.-464G>T
XM_011514062.3:c.19G>T	XP_011512364.1:p.Gly7Trp
XM_017009607.1:c.19G>T	XP_016865096.1:p.Gly7Trp
XM_017009608.2:c.19G>T	XP_016865097.1:p.Gly7Trp
XM_017009609.1:c.-142G>T	XP_016865098.1:n.-142G>T
XM_017009610.1:c.-556G>T	XP_016865099.1:n.-556G>T
XM_017009611.2:c.-553G>T	XP_016865100.1:n.-553G>T
XM_017009612.2:c.-464G>T	XP_016865101.1:n.-464G>T
XM_017009613.2:c.-556G>T	XP_016865102.1:n.-556G>T
XM_017009614.1:c.-649G>T	XP_016865103.1:n.-649G>T
XM_017009615.1:c.-557G>T	XP_016865104.1:n.-557G>T
XM_017009616.1:c.-461G>T	XP_016865105.1:n.-461G>T
NM_018356.3:c.19G>T MANE Select	NP_060826.2:p.Gly7Trp
NR_134298.2:n.111G>T