Canonical Allele Identifier: CA551377381
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1203138492

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091407_55091408del , CM000666.2:g.55091407_55091408del GRCh38
NC_000004.11:g.55957574_55957575del , CM000666.1:g.55957574_55957575del GRCh37
NC_000004.10:g.55652331_55652332del NCBI36
NG_012004.1:g.39188_39189del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+1209_3069+1210del MANE Select ENSP00000263923.4:n.3069+1209_3069+1210del
ENST00000647068.1:n.3082+1209_3082+1210del
ENST00000263923.4:c.3069+1209_3069+1210del ENSP00000263923.4:n.3069+1209_3069+1210del
NM_002253.2:c.3069+1209_3069+1210del NP_002244.1:n.3069+1209_3069+1210del
NM_002253.3:c.3069+1209_3069+1210del NP_002244.1:n.3069+1209_3069+1210del
NM_002253.4:c.3069+1209_3069+1210del MANE Select NP_002244.1:n.3069+1209_3069+1210del