Canonical Allele Identifier: CA1458933517
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112694A= , CM000666.2:g.55112694A= GRCh38
NC_000004.11:g.55978861A= , CM000666.1:g.55978861A= GRCh37
NC_000004.10:g.55673618A= NCBI36
NG_012004.1:g.17902T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.976+610T= MANE Select ENSP00000263923.4:n.976+610T=
ENST00000647068.1:n.989+610T=
ENST00000263923.4:c.976+610T= ENSP00000263923.4:n.976+610T=
ENST00000512566.1:n.976+610T=
NM_002253.2:c.976+610T= NP_002244.1:n.976+610T=
NM_002253.3:c.976+610T= NP_002244.1:n.976+610T=
NM_002253.4:c.976+610T= MANE Select NP_002244.1:n.976+610T=