Canonical Allele Identifier: CA1458932488
Gene: KDR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110546A= , CM000666.2:g.55110546A= GRCh38
NC_000004.11:g.55976713A= , CM000666.1:g.55976713A= GRCh37
NC_000004.10:g.55671470A= NCBI36
NG_012004.1:g.20050T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1112T= MANE Select ENSP00000263923.4:p.Leu371=
ENST00000647068.1:n.1125T=
ENST00000263923.4:c.1112T= ENSP00000263923.4:p.Leu371=
ENST00000512566.1:n.1112T=
NM_002253.2:c.1112T= NP_002244.1:p.Leu371=
NM_002253.3:c.1112T= NP_002244.1:p.Leu371=
NM_002253.4:c.1112T= MANE Select NP_002244.1:p.Leu371=
Search 100 bp 5'
Search 100 bp 3'