Canonical Allele Identifier: CA028787
Gene: CD244 HGNC NCBI

Linked Data

ClinVar Variation Id: 4895
ClinVar RCV Id: RCV000005173
dbSNP Id: rs3766379

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160837925T>C , CM000663.2:g.160837925T>C GRCh38
NC_000001.10:g.160807715T>C , CM000663.1:g.160807715T>C GRCh37
NC_000001.9:g.159074339T>C NCBI36
NG_015991.1:g.29978A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368034.9:c.834+526A>G MANE Select ENSP00000357013.4:n.834+526A>G
ENST00000322302.7:c.558+526A>G ENSP00000313619.7:n.558+526A>G
ENST00000368033.7:c.849+526A>G ENSP00000357012.3:n.849+526A>G
ENST00000368034.8:c.834+526A>G ENSP00000357013.4:n.834+526A>G
ENST00000481677.1:n.414+526A>G
ENST00000492063.5:c.834+526A>G ENSP00000432636.1:n.834+526A>G
NM_001166663.1:c.849+526A>G NP_001160135.1:n.849+526A>G
NM_001166664.1:c.558+526A>G NP_001160136.1:n.558+526A>G
NM_016382.3:c.834+526A>G NP_057466.1:n.834+526A>G
XM_011509620.1:c.849+526A>G XP_011507922.1:n.849+526A>G
XM_011509621.1:c.849+526A>G XP_011507923.1:n.849+526A>G
XM_011509622.1:c.834+526A>G XP_011507924.1:n.834+526A>G
XM_011509623.1:c.240+526A>G XP_011507925.1:n.240+526A>G
XM_011509621.2:c.849+526A>G XP_011507923.1:n.849+526A>G
XM_011509622.2:c.834+526A>G XP_011507924.1:n.834+526A>G
XM_011509623.3:c.240+526A>G XP_011507925.1:n.240+526A>G
XR_001737229.1:n.1178+526A>G
NM_016382.4:c.834+526A>G MANE Select NP_057466.1:n.834+526A>G
NM_001166663.2:c.849+526A>G NP_001160135.1:n.849+526A>G
NM_001166664.2:c.558+526A>G NP_001160136.1:n.558+526A>G