Canonical Allele Identifier: CA279882
Gene: CCDC22 HGNC NCBI

Linked Data

ClinVar Variation Id: 218105
ClinVar RCV Id: RCV000202354 RCV001028073
dbSNP Id: rs863225428
MyVariant Identifiers: chrX:g.49092145A>G (hg19) chrX:g.49235685A>G (hg38)
PubMed: PMID:19377476 PMID:21826058
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49235685A>G , CM000685.2:g.49235685A>G GRCh38
NC_000023.10:g.49092145A>G , CM000685.1:g.49092145A>G GRCh37
NC_000023.9:g.48979089A>G NCBI36
NG_009095.2:g.2682T>C
NG_021311.2:g.5221A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376227.4:c.49A>G MANE Select ENSP00000365401.3:p.Thr17Ala
ENST00000376227.3:c.49A>G ENSP00000365401.3:p.Thr17Ala
ENST00000496651.5:n.190A>G
NM_014008.4:c.49A>G NP_054727.1:p.Thr17Ala
XM_005272599.2:c.49A>G XP_005272656.1:p.Thr17Ala
XR_430506.1:n.151A>G
XM_005272599.4:c.49A>G XP_005272656.1:p.Thr17Ala
XR_430506.3:n.164A>G
NM_014008.5:c.49A>G MANE Select NP_054727.1:p.Thr17Ala
Search 100 bp 5'
Search 100 bp 3'