Canonical Allele Identifier: CA1202488526

Gene: CD244

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160837899_160837926delinsGCAGGCGAGAGGCTCCTGGAGGAGCCTA , CM000663.2:g.160837899_160837926delinsGCAGGCGAGAGGCTCCTGGAGGAGCCTA	GRCh38
NC_000001.10:g.160807689_160807716delinsGCAGGCGAGAGGCTCCTGGAGGAGCCTA , CM000663.1:g.160807689_160807716delinsGCAGGCGAGAGGCTCCTGGAGGAGCCTA	GRCh37
NC_000001.9:g.159074313_159074340delinsGCAGGCGAGAGGCTCCTGGAGGAGCCTA	NCBI36
NG_015991.1:g.29977_30004delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368034.9:c.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC MANE Select	ENSP00000357013.4:n.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTC...
ENST00000322302.7:c.558+525_558+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	ENSP00000313619.7:n.558+525_558+552delinsTAGGCTCCTCCAGGAGCCTC...
ENST00000368033.7:c.849+525_849+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	ENSP00000357012.3:n.849+525_849+552delinsTAGGCTCCTCCAGGAGCCTC...
ENST00000368034.8:c.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	ENSP00000357013.4:n.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTC...
ENST00000481677.1:n.414+525_414+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC
ENST00000492063.5:c.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	ENSP00000432636.1:n.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTC...
NM_001166663.1:c.849+525_849+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	NP_001160135.1:n.849+525_849+552delinsTAGGCTCCTCCAGGAGCCTCTCG...
NM_001166664.1:c.558+525_558+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	NP_001160136.1:n.558+525_558+552delinsTAGGCTCCTCCAGGAGCCTCTCG...
NM_016382.3:c.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	NP_057466.1:n.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCT...
XM_011509620.1:c.849+525_849+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	XP_011507922.1:n.849+525_849+552delinsTAGGCTCCTCCAGGAGCCTCTCG...
XM_011509621.1:c.849+525_849+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	XP_011507923.1:n.849+525_849+552delinsTAGGCTCCTCCAGGAGCCTCTCG...
XM_011509622.1:c.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	XP_011507924.1:n.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTCTCG...
XM_011509623.1:c.240+525_240+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	XP_011507925.1:n.240+525_240+552delinsTAGGCTCCTCCAGGAGCCTCTCG...
XM_011509621.2:c.849+525_849+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	XP_011507923.1:n.849+525_849+552delinsTAGGCTCCTCCAGGAGCCTCTCG...
XM_011509622.2:c.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	XP_011507924.1:n.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTCTCG...
XM_011509623.3:c.240+525_240+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	XP_011507925.1:n.240+525_240+552delinsTAGGCTCCTCCAGGAGCCTCTCG...
XR_001737229.1:n.1178+525_1178+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC
NM_016382.4:c.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC MANE Select	NP_057466.1:n.834+525_834+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCT...
NM_001166663.2:c.849+525_849+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	NP_001160135.1:n.849+525_849+552delinsTAGGCTCCTCCAGGAGCCTCTCG...
NM_001166664.2:c.558+525_558+552delinsTAGGCTCCTCCAGGAGCCTCTCGCCTGC	NP_001160136.1:n.558+525_558+552delinsTAGGCTCCTCCAGGAGCCTCTCG...