Canonical Allele Identifier: CA558448110

Gene: C5orf22

Linked Data

• dbSNP Id: rs1281192953
• gnomAD v2: 5-31532444-T-C
• gnomAD v3: 5-31532337-T-C
• gnomAD v4: 5-31532337-T-C
• MyVariant Identifiers: chr5:g.31532444T>C (hg19) ; chr5:g.31532337T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.31532337T>C , CM000667.2:g.31532337T>C	GRCh38
NC_000005.9:g.31532444T>C , CM000667.1:g.31532444T>C	GRCh37
NC_000005.8:g.31568201T>C	NCBI36
NG_051574.1:g.4839A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325366.14:c.-56T>C MANE Select	ENSP00000326879.9:n.-56T>C
ENST00000325366.13:c.-56T>C	ENSP00000326879.9:n.-56T>C
ENST00000504464.5:c.-56T>C	ENSP00000430261.1:n.-56T>C
ENST00000507818.6:c.-56T>C	ENSP00000430860.1:n.-56T>C
ENST00000510659.5:c.-56T>C	ENSP00000423039.1:n.-56T>C
ENST00000511208.2:c.-56T>C	ENSP00000428898.1:n.-56T>C
ENST00000513967.5:c.-56T>C	ENSP00000421667.1:n.-56T>C
ENST00000515409.5:n.43T>C
ENST00000517780.1:n.43T>C
NM_018356.2:c.-56T>C	NP_060826.2:n.-56T>C
XM_005248319.2:c.-627T>C	XP_005248376.1:n.-627T>C
XM_006714479.1:c.-216T>C	XP_006714542.1:n.-216T>C
XM_006714480.2:c.-538T>C	XP_006714543.1:n.-538T>C
XM_011514062.1:c.-56T>C	XP_011512364.1:n.-56T>C
NR_134298.1:n.72T>C
XM_006714479.2:c.-216T>C	XP_006714542.1:n.-216T>C
XM_006714480.3:c.-538T>C	XP_006714543.1:n.-538T>C
XM_011514062.3:c.-56T>C	XP_011512364.1:n.-56T>C
XM_017009607.1:c.-56T>C	XP_016865096.1:n.-56T>C
XM_017009608.2:c.-56T>C	XP_016865097.1:n.-56T>C
XM_017009609.1:c.-216T>C	XP_016865098.1:n.-216T>C
XM_017009610.1:c.-630T>C	XP_016865099.1:n.-630T>C
XM_017009611.2:c.-627T>C	XP_016865100.1:n.-627T>C
XM_017009612.2:c.-538T>C	XP_016865101.1:n.-538T>C
XM_017009613.2:c.-630T>C	XP_016865102.1:n.-630T>C
XM_017009614.1:c.-723T>C	XP_016865103.1:n.-723T>C
XM_017009615.1:c.-631T>C	XP_016865104.1:n.-631T>C
XM_017009616.1:c.-535T>C	XP_016865105.1:n.-535T>C
NM_018356.3:c.-56T>C MANE Select	NP_060826.2:n.-56T>C
NR_134298.2:n.37T>C