Canonical Allele Identifier: CA796406977
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1315070068

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55124932_55124946del , CM000666.2:g.55124932_55124946del GRCh38
NC_000004.11:g.55991099_55991113del , CM000666.1:g.55991099_55991113del GRCh37
NC_000004.10:g.55685856_55685870del NCBI36
NG_012004.1:g.5651_5665del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+282_67+296del MANE Select ENSP00000263923.4:n.67+282_67+296del
ENST00000263923.4:c.67+282_67+296del ENSP00000263923.4:n.67+282_67+296del
ENST00000512566.1:n.67+282_67+296del
NM_002253.2:c.67+282_67+296del NP_002244.1:n.67+282_67+296del
NM_002253.3:c.67+282_67+296del NP_002244.1:n.67+282_67+296del
NM_002253.4:c.67+282_67+296del MANE Select NP_002244.1:n.67+282_67+296del