Canonical Allele Identifier: CA31588855

Gene: CD244

Linked Data

• dbSNP Id: rs748780628
• MyVariant Identifiers: chr1:g.160807750_160807751del (hg19) ; chr1:g.160837960_160837961del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160837966_160837967del , CM000663.2:g.160837966_160837967del	GRCh38
NC_000001.10:g.160807756_160807757del , CM000663.1:g.160807756_160807757del	GRCh37
NC_000001.9:g.159074380_159074381del	NCBI36
NG_015991.1:g.29942_29943del

Transcript Alleles

HGVS	Amino-acid change
ENST00000368034.9:c.834+490_834+491del MANE Select	ENSP00000357013.4:n.834+490_834+491del
ENST00000322302.7:c.558+490_558+491del	ENSP00000313619.7:n.558+490_558+491del
ENST00000368033.7:c.849+490_849+491del	ENSP00000357012.3:n.849+490_849+491del
ENST00000368034.8:c.834+490_834+491del	ENSP00000357013.4:n.834+490_834+491del
ENST00000481677.1:n.414+490_414+491del
ENST00000492063.5:c.834+490_834+491del	ENSP00000432636.1:n.834+490_834+491del
NM_001166663.1:c.849+490_849+491del	NP_001160135.1:n.849+490_849+491del
NM_001166664.1:c.558+490_558+491del	NP_001160136.1:n.558+490_558+491del
NM_016382.3:c.834+490_834+491del	NP_057466.1:n.834+490_834+491del
XM_011509620.1:c.849+490_849+491del	XP_011507922.1:n.849+490_849+491del
XM_011509621.1:c.849+490_849+491del	XP_011507923.1:n.849+490_849+491del
XM_011509622.1:c.834+490_834+491del	XP_011507924.1:n.834+490_834+491del
XM_011509623.1:c.240+490_240+491del	XP_011507925.1:n.240+490_240+491del
XM_011509621.2:c.849+490_849+491del	XP_011507923.1:n.849+490_849+491del
XM_011509622.2:c.834+490_834+491del	XP_011507924.1:n.834+490_834+491del
XM_011509623.3:c.240+490_240+491del	XP_011507925.1:n.240+490_240+491del
XR_001737229.1:n.1178+490_1178+491del
NM_016382.4:c.834+490_834+491del MANE Select	NP_057466.1:n.834+490_834+491del
NM_001166663.2:c.849+490_849+491del	NP_001160135.1:n.849+490_849+491del
NM_001166664.2:c.558+490_558+491del	NP_001160136.1:n.558+490_558+491del