Canonical Allele Identifier: CA96884069
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs386674535

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091407_55091416delinsT , CM000666.2:g.55091407_55091416delinsT GRCh38
NC_000004.11:g.55957574_55957583delinsT , CM000666.1:g.55957574_55957583delinsT GRCh37
NC_000004.10:g.55652331_55652340delinsT NCBI36
NG_012004.1:g.39180_39189delinsA

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+1201_3069+1210delinsA MANE Select ENSP00000263923.4:n.3069+1201_3069+1210delinsA
ENST00000647068.1:n.3082+1201_3082+1210delinsA
ENST00000263923.4:c.3069+1201_3069+1210delinsA ENSP00000263923.4:n.3069+1201_3069+1210delinsA
NM_002253.2:c.3069+1201_3069+1210delinsA NP_002244.1:n.3069+1201_3069+1210delinsA
NM_002253.3:c.3069+1201_3069+1210delinsA NP_002244.1:n.3069+1201_3069+1210delinsA
NM_002253.4:c.3069+1201_3069+1210delinsA MANE Select NP_002244.1:n.3069+1201_3069+1210delinsA