Canonical Allele Identifier: CA1458933202
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112090A= , CM000666.2:g.55112090A= GRCh38
NC_000004.11:g.55978257A= , CM000666.1:g.55978257A= GRCh37
NC_000004.10:g.55673014A= NCBI36
NG_012004.1:g.18506T=

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.976+1214T= MANE Select ENSP00000263923.4:n.976+1214T=
ENST00000647068.1:n.989+1214T=
ENST00000263923.4:c.976+1214T= ENSP00000263923.4:n.976+1214T=
ENST00000512566.1:n.976+1214T=
NM_002253.2:c.976+1214T= NP_002244.1:n.976+1214T=
NM_002253.3:c.976+1214T= NP_002244.1:n.976+1214T=
NM_002253.4:c.976+1214T= MANE Select NP_002244.1:n.976+1214T=