Canonical Allele Identifier: CA526860876

Gene: CD244

Linked Data

• dbSNP Id: rs1289683467
• gnomAD v2: 1-160807668-GGCCCC-G
• gnomAD v3: 1-160837878-GGCCCC-G
• gnomAD v4: 1-160837878-GGCCCC-G
• MyVariant Identifiers: chr1:g.160807669_160807673del (hg19) ; chr1:g.160837879_160837883del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160837879_160837883del , CM000663.2:g.160837879_160837883del	GRCh38
NC_000001.10:g.160807669_160807673del , CM000663.1:g.160807669_160807673del	GRCh37
NC_000001.9:g.159074293_159074297del	NCBI36
NG_015991.1:g.30020_30024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368034.9:c.834+568_834+572del MANE Select	ENSP00000357013.4:n.834+568_834+572del
ENST00000322302.7:c.558+568_558+572del	ENSP00000313619.7:n.558+568_558+572del
ENST00000368033.7:c.849+568_849+572del	ENSP00000357012.3:n.849+568_849+572del
ENST00000368034.8:c.834+568_834+572del	ENSP00000357013.4:n.834+568_834+572del
ENST00000481677.1:n.414+568_414+572del
ENST00000492063.5:c.834+568_834+572del	ENSP00000432636.1:n.834+568_834+572del
NM_001166663.1:c.849+568_849+572del	NP_001160135.1:n.849+568_849+572del
NM_001166664.1:c.558+568_558+572del	NP_001160136.1:n.558+568_558+572del
NM_016382.3:c.834+568_834+572del	NP_057466.1:n.834+568_834+572del
XM_011509620.1:c.849+568_849+572del	XP_011507922.1:n.849+568_849+572del
XM_011509621.1:c.849+568_849+572del	XP_011507923.1:n.849+568_849+572del
XM_011509622.1:c.834+568_834+572del	XP_011507924.1:n.834+568_834+572del
XM_011509623.1:c.240+568_240+572del	XP_011507925.1:n.240+568_240+572del
XM_011509621.2:c.849+568_849+572del	XP_011507923.1:n.849+568_849+572del
XM_011509622.2:c.834+568_834+572del	XP_011507924.1:n.834+568_834+572del
XM_011509623.3:c.240+568_240+572del	XP_011507925.1:n.240+568_240+572del
XR_001737229.1:n.1178+568_1178+572del
NM_016382.4:c.834+568_834+572del MANE Select	NP_057466.1:n.834+568_834+572del
NM_001166663.2:c.849+568_849+572del	NP_001160135.1:n.849+568_849+572del
NM_001166664.2:c.558+568_558+572del	NP_001160136.1:n.558+568_558+572del