Canonical Allele Identifier: CA1458911664
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096549A= , CM000666.2:g.55096549A= GRCh38
NC_000004.11:g.55962716A= , CM000666.1:g.55962716A= GRCh37
NC_000004.10:g.55657473A= NCBI36
NG_012004.1:g.34047T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-207T= MANE Select ENSP00000263923.4:n.2615-207T=
ENST00000647068.1:n.2628-207T=
ENST00000263923.4:c.2615-207T= ENSP00000263923.4:n.2615-207T=
ENST00000509309.1:n.172T=
NM_002253.2:c.2615-207T= NP_002244.1:n.2615-207T=
NM_002253.3:c.2615-207T= NP_002244.1:n.2615-207T=
NM_002253.4:c.2615-207T= MANE Select NP_002244.1:n.2615-207T=