Canonical Allele Identifier: CA1008368752

Gene: CD244

Linked Data

• dbSNP Id: rs1669385632
• gnomAD v3: 1-160837804-GAC-G
• gnomAD v4: 1-160837804-GAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160837808_160837809del , CM000663.2:g.160837808_160837809del	GRCh38
NC_000001.10:g.160807598_160807599del , CM000663.1:g.160807598_160807599del	GRCh37
NC_000001.9:g.159074222_159074223del	NCBI36
NG_015991.1:g.30097_30098del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368034.9:c.834+645_834+646del MANE Select	ENSP00000357013.4:n.834+645_834+646del
ENST00000322302.7:c.558+645_558+646del	ENSP00000313619.7:n.558+645_558+646del
ENST00000368033.7:c.849+645_849+646del	ENSP00000357012.3:n.849+645_849+646del
ENST00000368034.8:c.834+645_834+646del	ENSP00000357013.4:n.834+645_834+646del
ENST00000481677.1:n.414+645_414+646del
ENST00000492063.5:c.834+645_834+646del	ENSP00000432636.1:n.834+645_834+646del
NM_001166663.1:c.849+645_849+646del	NP_001160135.1:n.849+645_849+646del
NM_001166664.1:c.558+645_558+646del	NP_001160136.1:n.558+645_558+646del
NM_016382.3:c.834+645_834+646del	NP_057466.1:n.834+645_834+646del
XM_011509620.1:c.849+645_849+646del	XP_011507922.1:n.849+645_849+646del
XM_011509621.1:c.849+645_849+646del	XP_011507923.1:n.849+645_849+646del
XM_011509622.1:c.834+645_834+646del	XP_011507924.1:n.834+645_834+646del
XM_011509623.1:c.240+645_240+646del	XP_011507925.1:n.240+645_240+646del
XM_011509621.2:c.849+645_849+646del	XP_011507923.1:n.849+645_849+646del
XM_011509622.2:c.834+645_834+646del	XP_011507924.1:n.834+645_834+646del
XM_011509623.3:c.240+645_240+646del	XP_011507925.1:n.240+645_240+646del
XR_001737229.1:n.1178+645_1178+646del
NM_016382.4:c.834+645_834+646del MANE Select	NP_057466.1:n.834+645_834+646del
NM_001166663.2:c.849+645_849+646del	NP_001160135.1:n.849+645_849+646del
NM_001166664.2:c.558+645_558+646del	NP_001160136.1:n.558+645_558+646del