Canonical Allele Identifier: CA1458933498
Gene: KDR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112657T= , CM000666.2:g.55112657T= GRCh38
NC_000004.11:g.55978824T= , CM000666.1:g.55978824T= GRCh37
NC_000004.10:g.55673581T= NCBI36
NG_012004.1:g.17939A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.976+647A= MANE Select ENSP00000263923.4:n.976+647A=
ENST00000647068.1:n.989+647A=
ENST00000263923.4:c.976+647A= ENSP00000263923.4:n.976+647A=
ENST00000512566.1:n.976+647A=
NM_002253.2:c.976+647A= NP_002244.1:n.976+647A=
NM_002253.3:c.976+647A= NP_002244.1:n.976+647A=
NM_002253.4:c.976+647A= MANE Select NP_002244.1:n.976+647A=
Search 100 bp 5'
Search 100 bp 3'