Canonical Allele Identifier: CA526860883

Gene: CD244

Linked Data

• dbSNP Id: rs1485397265
• gnomAD v2: 1-160807678-TGCTG-T
• gnomAD v3: 1-160837888-TGCTG-T
• gnomAD v4: 1-160837888-TGCTG-T
• MyVariant Identifiers: chr1:g.160807679_160807682del (hg19) ; chr1:g.160837889_160837892del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160837889_160837892del , CM000663.2:g.160837889_160837892del	GRCh38
NC_000001.10:g.160807679_160807682del , CM000663.1:g.160807679_160807682del	GRCh37
NC_000001.9:g.159074303_159074306del	NCBI36
NG_015991.1:g.30011_30014del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368034.9:c.834+559_834+562del MANE Select	ENSP00000357013.4:n.834+559_834+562del
ENST00000322302.7:c.558+559_558+562del	ENSP00000313619.7:n.558+559_558+562del
ENST00000368033.7:c.849+559_849+562del	ENSP00000357012.3:n.849+559_849+562del
ENST00000368034.8:c.834+559_834+562del	ENSP00000357013.4:n.834+559_834+562del
ENST00000481677.1:n.414+559_414+562del
ENST00000492063.5:c.834+559_834+562del	ENSP00000432636.1:n.834+559_834+562del
NM_001166663.1:c.849+559_849+562del	NP_001160135.1:n.849+559_849+562del
NM_001166664.1:c.558+559_558+562del	NP_001160136.1:n.558+559_558+562del
NM_016382.3:c.834+559_834+562del	NP_057466.1:n.834+559_834+562del
XM_011509620.1:c.849+559_849+562del	XP_011507922.1:n.849+559_849+562del
XM_011509621.1:c.849+559_849+562del	XP_011507923.1:n.849+559_849+562del
XM_011509622.1:c.834+559_834+562del	XP_011507924.1:n.834+559_834+562del
XM_011509623.1:c.240+559_240+562del	XP_011507925.1:n.240+559_240+562del
XM_011509621.2:c.849+559_849+562del	XP_011507923.1:n.849+559_849+562del
XM_011509622.2:c.834+559_834+562del	XP_011507924.1:n.834+559_834+562del
XM_011509623.3:c.240+559_240+562del	XP_011507925.1:n.240+559_240+562del
XR_001737229.1:n.1178+559_1178+562del
NM_016382.4:c.834+559_834+562del MANE Select	NP_057466.1:n.834+559_834+562del
NM_001166663.2:c.849+559_849+562del	NP_001160135.1:n.849+559_849+562del
NM_001166664.2:c.558+559_558+562del	NP_001160136.1:n.558+559_558+562del