Canonical Allele Identifier: CA1202488585
Gene: CD244 HGNC NCBI

Linked Data

dbSNP Id: rs1669393727

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160838028C>G , CM000663.2:g.160838028C>G GRCh38
NC_000001.10:g.160807818C>G , CM000663.1:g.160807818C>G GRCh37
NC_000001.9:g.159074442C>G NCBI36
NG_015991.1:g.29875G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368034.9:c.834+423G>C MANE Select ENSP00000357013.4:n.834+423G>C
ENST00000322302.7:c.558+423G>C ENSP00000313619.7:n.558+423G>C
ENST00000368033.7:c.849+423G>C ENSP00000357012.3:n.849+423G>C
ENST00000368034.8:c.834+423G>C ENSP00000357013.4:n.834+423G>C
ENST00000481677.1:n.414+423G>C
ENST00000492063.5:c.834+423G>C ENSP00000432636.1:n.834+423G>C
NM_001166663.1:c.849+423G>C NP_001160135.1:n.849+423G>C
NM_001166664.1:c.558+423G>C NP_001160136.1:n.558+423G>C
NM_016382.3:c.834+423G>C NP_057466.1:n.834+423G>C
XM_011509620.1:c.849+423G>C XP_011507922.1:n.849+423G>C
XM_011509621.1:c.849+423G>C XP_011507923.1:n.849+423G>C
XM_011509622.1:c.834+423G>C XP_011507924.1:n.834+423G>C
XM_011509623.1:c.240+423G>C XP_011507925.1:n.240+423G>C
XM_011509621.2:c.849+423G>C XP_011507923.1:n.849+423G>C
XM_011509622.2:c.834+423G>C XP_011507924.1:n.834+423G>C
XM_011509623.3:c.240+423G>C XP_011507925.1:n.240+423G>C
XR_001737229.1:n.1178+423G>C
NM_016382.4:c.834+423G>C MANE Select NP_057466.1:n.834+423G>C
NM_001166663.2:c.849+423G>C NP_001160135.1:n.849+423G>C
NM_001166664.2:c.558+423G>C NP_001160136.1:n.558+423G>C