Canonical Allele Identifier: CA1458940111
Gene: KDR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125208T= , CM000666.2:g.55125208T= GRCh38
NC_000004.11:g.55991375T= , CM000666.1:g.55991375T= GRCh37
NC_000004.10:g.55686132T= NCBI36
NG_012004.1:g.5388A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+19A= MANE Select ENSP00000263923.4:n.67+19A=
ENST00000263923.4:c.67+19A= ENSP00000263923.4:n.67+19A=
ENST00000512566.1:n.67+19A=
NM_002253.2:c.67+19A= NP_002244.1:n.67+19A=
NM_002253.3:c.67+19A= NP_002244.1:n.67+19A=
NM_002253.4:c.67+19A= MANE Select NP_002244.1:n.67+19A=
Search 100 bp 5'
Search 100 bp 3'