Canonical Allele Identifier: CA796407039
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1291961441

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125020_55125059del , CM000666.2:g.55125020_55125059del GRCh38
NC_000004.11:g.55991187_55991226del , CM000666.1:g.55991187_55991226del GRCh37
NC_000004.10:g.55685944_55685983del NCBI36
NG_012004.1:g.5539_5578del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+170_67+209del MANE Select ENSP00000263923.4:n.67+170_67+209del
ENST00000263923.4:c.67+170_67+209del ENSP00000263923.4:n.67+170_67+209del
ENST00000512566.1:n.67+170_67+209del
NM_002253.2:c.67+170_67+209del NP_002244.1:n.67+170_67+209del
NM_002253.3:c.67+170_67+209del NP_002244.1:n.67+170_67+209del
NM_002253.4:c.67+170_67+209del MANE Select NP_002244.1:n.67+170_67+209del