Canonical Allele Identifier: CA1202488568

Gene: CD244

Linked Data

• dbSNP Id: rs1669392472

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160837996_160837998del , CM000663.2:g.160837996_160837998del	GRCh38
NC_000001.10:g.160807786_160807788del , CM000663.1:g.160807786_160807788del	GRCh37
NC_000001.9:g.159074410_159074412del	NCBI36
NG_015991.1:g.29910_29912del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368034.9:c.834+458_834+460del MANE Select	ENSP00000357013.4:n.834+458_834+460del
ENST00000322302.7:c.558+458_558+460del	ENSP00000313619.7:n.558+458_558+460del
ENST00000368033.7:c.849+458_849+460del	ENSP00000357012.3:n.849+458_849+460del
ENST00000368034.8:c.834+458_834+460del	ENSP00000357013.4:n.834+458_834+460del
ENST00000481677.1:n.414+458_414+460del
ENST00000492063.5:c.834+458_834+460del	ENSP00000432636.1:n.834+458_834+460del
NM_001166663.1:c.849+458_849+460del	NP_001160135.1:n.849+458_849+460del
NM_001166664.1:c.558+458_558+460del	NP_001160136.1:n.558+458_558+460del
NM_016382.3:c.834+458_834+460del	NP_057466.1:n.834+458_834+460del
XM_011509620.1:c.849+458_849+460del	XP_011507922.1:n.849+458_849+460del
XM_011509621.1:c.849+458_849+460del	XP_011507923.1:n.849+458_849+460del
XM_011509622.1:c.834+458_834+460del	XP_011507924.1:n.834+458_834+460del
XM_011509623.1:c.240+458_240+460del	XP_011507925.1:n.240+458_240+460del
XM_011509621.2:c.849+458_849+460del	XP_011507923.1:n.849+458_849+460del
XM_011509622.2:c.834+458_834+460del	XP_011507924.1:n.834+458_834+460del
XM_011509623.3:c.240+458_240+460del	XP_011507925.1:n.240+458_240+460del
XR_001737229.1:n.1178+458_1178+460del
NM_016382.4:c.834+458_834+460del MANE Select	NP_057466.1:n.834+458_834+460del
NM_001166663.2:c.849+458_849+460del	NP_001160135.1:n.849+458_849+460del
NM_001166664.2:c.558+458_558+460del	NP_001160136.1:n.558+458_558+460del