Canonical Allele Identifier: CA1458928348
Gene: KDR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091655G= , CM000666.2:g.55091655G= GRCh38
NC_000004.11:g.55957822G= , CM000666.1:g.55957822G= GRCh37
NC_000004.10:g.55652579G= NCBI36
NG_012004.1:g.38941C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+962C= MANE Select ENSP00000263923.4:n.3069+962C=
ENST00000647068.1:n.3082+962C=
ENST00000263923.4:c.3069+962C= ENSP00000263923.4:n.3069+962C=
NM_002253.2:c.3069+962C= NP_002244.1:n.3069+962C=
NM_002253.3:c.3069+962C= NP_002244.1:n.3069+962C=
NM_002253.4:c.3069+962C= MANE Select NP_002244.1:n.3069+962C=
Search 100 bp 5'
Search 100 bp 3'