Canonical Allele Identifier: CA1458928227
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091445A= , CM000666.2:g.55091445A= GRCh38
NC_000004.11:g.55957612A= , CM000666.1:g.55957612A= GRCh37
NC_000004.10:g.55652369A= NCBI36
NG_012004.1:g.39151T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+1172T= MANE Select ENSP00000263923.4:n.3069+1172T=
ENST00000647068.1:n.3082+1172T=
ENST00000263923.4:c.3069+1172T= ENSP00000263923.4:n.3069+1172T=
NM_002253.2:c.3069+1172T= NP_002244.1:n.3069+1172T=
NM_002253.3:c.3069+1172T= NP_002244.1:n.3069+1172T=
NM_002253.4:c.3069+1172T= MANE Select NP_002244.1:n.3069+1172T=