Canonical Allele Identifier: CA1458911708
Gene: KDR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096611C= , CM000666.2:g.55096611C= GRCh38
NC_000004.11:g.55962778C= , CM000666.1:g.55962778C= GRCh37
NC_000004.10:g.55657535C= NCBI36
NG_012004.1:g.33985G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-269G= MANE Select ENSP00000263923.4:n.2615-269G=
ENST00000647068.1:n.2628-269G=
ENST00000263923.4:c.2615-269G= ENSP00000263923.4:n.2615-269G=
ENST00000509309.1:n.110G=
NM_002253.2:c.2615-269G= NP_002244.1:n.2615-269G=
NM_002253.3:c.2615-269G= NP_002244.1:n.2615-269G=
NM_002253.4:c.2615-269G= MANE Select NP_002244.1:n.2615-269G=
Search 100 bp 5'
Search 100 bp 3'