Canonical Allele Identifier: CA796419734
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs386674535

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091408_55091416del , CM000666.2:g.55091408_55091416del GRCh38
NC_000004.11:g.55957575_55957583del , CM000666.1:g.55957575_55957583del GRCh37
NC_000004.10:g.55652332_55652340del NCBI36
NG_012004.1:g.39181_39189del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+1202_3069+1210del MANE Select ENSP00000263923.4:n.3069+1202_3069+1210del
ENST00000647068.1:n.3082+1202_3082+1210del
ENST00000263923.4:c.3069+1202_3069+1210del ENSP00000263923.4:n.3069+1202_3069+1210del
NM_002253.2:c.3069+1202_3069+1210del NP_002244.1:n.3069+1202_3069+1210del
NM_002253.3:c.3069+1202_3069+1210del NP_002244.1:n.3069+1202_3069+1210del
NM_002253.4:c.3069+1202_3069+1210del MANE Select NP_002244.1:n.3069+1202_3069+1210del