Canonical Allele Identifier: CA1458911610
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096457T= , CM000666.2:g.55096457T= GRCh38
NC_000004.11:g.55962624T= , CM000666.1:g.55962624T= GRCh37
NC_000004.10:g.55657381T= NCBI36
NG_012004.1:g.34139A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-115A= MANE Select ENSP00000263923.4:n.2615-115A=
ENST00000647068.1:n.2628-115A=
ENST00000263923.4:c.2615-115A= ENSP00000263923.4:n.2615-115A=
ENST00000509309.1:n.264A=
NM_002253.2:c.2615-115A= NP_002244.1:n.2615-115A=
NM_002253.3:c.2615-115A= NP_002244.1:n.2615-115A=
NM_002253.4:c.2615-115A= MANE Select NP_002244.1:n.2615-115A=