Canonical Allele Identifier: CA1458928345
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091648G= , CM000666.2:g.55091648G= GRCh38
NC_000004.11:g.55957815G= , CM000666.1:g.55957815G= GRCh37
NC_000004.10:g.55652572G= NCBI36
NG_012004.1:g.38948C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+969C= MANE Select ENSP00000263923.4:n.3069+969C=
ENST00000647068.1:n.3082+969C=
ENST00000263923.4:c.3069+969C= ENSP00000263923.4:n.3069+969C=
NM_002253.2:c.3069+969C= NP_002244.1:n.3069+969C=
NM_002253.3:c.3069+969C= NP_002244.1:n.3069+969C=
NM_002253.4:c.3069+969C= MANE Select NP_002244.1:n.3069+969C=