Canonical Allele Identifier: CA251260
Gene: KDR HGNC NCBI

Linked Data

ClinVar Variation Id: 204332
ClinVar RCV Id: RCV000186523
dbSNP Id: rs795902898
MyVariant Identifiers: chr4:g.55963960del (hg19) chr4:g.55097793del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55097796del , CM000666.2:g.55097796del GRCh38
NC_000004.11:g.55963963del , CM000666.1:g.55963963del GRCh37
NC_000004.10:g.55658720del NCBI36
NG_012004.1:g.32803del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2510-27del MANE Select ENSP00000263923.4:n.2510-27del
ENST00000647068.1:n.2523-27del
ENST00000263923.4:c.2510-27del ENSP00000263923.4:n.2510-27del
NM_002253.2:c.2510-27del NP_002244.1:n.2510-27del
NM_002253.3:c.2510-27del NP_002244.1:n.2510-27del
NM_002253.4:c.2510-27del MANE Select NP_002244.1:n.2510-27del
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