Canonical Allele Identifier: CA1458911693
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096585_55096586delinsCT , CM000666.2:g.55096585_55096586delinsCT GRCh38
NC_000004.11:g.55962752_55962753delinsCT , CM000666.1:g.55962752_55962753delinsCT GRCh37
NC_000004.10:g.55657509_55657510delinsCT NCBI36
NG_012004.1:g.34010_34011delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-244_2615-243delinsAG MANE Select ENSP00000263923.4:n.2615-244_2615-243delinsAG
ENST00000647068.1:n.2628-244_2628-243delinsAG
ENST00000263923.4:c.2615-244_2615-243delinsAG ENSP00000263923.4:n.2615-244_2615-243delinsAG
ENST00000509309.1:n.135_136delinsAG
NM_002253.2:c.2615-244_2615-243delinsAG NP_002244.1:n.2615-244_2615-243delinsAG
NM_002253.3:c.2615-244_2615-243delinsAG NP_002244.1:n.2615-244_2615-243delinsAG
NM_002253.4:c.2615-244_2615-243delinsAG MANE Select NP_002244.1:n.2615-244_2615-243delinsAG