Canonical Allele Identifier: CA526860878

Gene: CD244

Linked Data

• dbSNP Id: rs1361872633
• gnomAD v2: 1-160807674-TGC-T
• gnomAD v3: 1-160837884-TGC-T
• gnomAD v4: 1-160837884-TGC-T
• MyVariant Identifiers: chr1:g.160807675_160807676del (hg19) ; chr1:g.160837885_160837886del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160837885_160837886del , CM000663.2:g.160837885_160837886del	GRCh38
NC_000001.10:g.160807675_160807676del , CM000663.1:g.160807675_160807676del	GRCh37
NC_000001.9:g.159074299_159074300del	NCBI36
NG_015991.1:g.30017_30018del

Transcript Alleles

HGVS	Amino-acid change
ENST00000368034.9:c.834+565_834+566del MANE Select	ENSP00000357013.4:n.834+565_834+566del
ENST00000322302.7:c.558+565_558+566del	ENSP00000313619.7:n.558+565_558+566del
ENST00000368033.7:c.849+565_849+566del	ENSP00000357012.3:n.849+565_849+566del
ENST00000368034.8:c.834+565_834+566del	ENSP00000357013.4:n.834+565_834+566del
ENST00000481677.1:n.414+565_414+566del
ENST00000492063.5:c.834+565_834+566del	ENSP00000432636.1:n.834+565_834+566del
NM_001166663.1:c.849+565_849+566del	NP_001160135.1:n.849+565_849+566del
NM_001166664.1:c.558+565_558+566del	NP_001160136.1:n.558+565_558+566del
NM_016382.3:c.834+565_834+566del	NP_057466.1:n.834+565_834+566del
XM_011509620.1:c.849+565_849+566del	XP_011507922.1:n.849+565_849+566del
XM_011509621.1:c.849+565_849+566del	XP_011507923.1:n.849+565_849+566del
XM_011509622.1:c.834+565_834+566del	XP_011507924.1:n.834+565_834+566del
XM_011509623.1:c.240+565_240+566del	XP_011507925.1:n.240+565_240+566del
XM_011509621.2:c.849+565_849+566del	XP_011507923.1:n.849+565_849+566del
XM_011509622.2:c.834+565_834+566del	XP_011507924.1:n.834+565_834+566del
XM_011509623.3:c.240+565_240+566del	XP_011507925.1:n.240+565_240+566del
XR_001737229.1:n.1178+565_1178+566del
NM_016382.4:c.834+565_834+566del MANE Select	NP_057466.1:n.834+565_834+566del
NM_001166663.2:c.849+565_849+566del	NP_001160135.1:n.849+565_849+566del
NM_001166664.2:c.558+565_558+566del	NP_001160136.1:n.558+565_558+566del