Canonical Allele Identifier: CA1458932519
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1720554673

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110598_55110601del , CM000666.2:g.55110598_55110601del GRCh38
NC_000004.11:g.55976765_55976768del , CM000666.1:g.55976765_55976768del GRCh37
NC_000004.10:g.55671522_55671525del NCBI36
NG_012004.1:g.19996_19999del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1092-34_1092-31del MANE Select ENSP00000263923.4:n.1092-34_1092-31del
ENST00000647068.1:n.1105-34_1105-31del
ENST00000263923.4:c.1092-34_1092-31del ENSP00000263923.4:n.1092-34_1092-31del
ENST00000512566.1:n.1092-34_1092-31del
NM_002253.2:c.1092-34_1092-31del NP_002244.1:n.1092-34_1092-31del
NM_002253.3:c.1092-34_1092-31del NP_002244.1:n.1092-34_1092-31del
NM_002253.4:c.1092-34_1092-31del MANE Select NP_002244.1:n.1092-34_1092-31del