Canonical Allele Identifier: CA796407471
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1267248026
gnomAD v3: 4-55125452-T-TG
gnomAD v4: 4-55125452-T-TG
MyVariant Identifiers: chr4:g.55991619_55991620insG (hg19) chr4:g.55125452_55125453insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125453dup , CM000666.2:g.55125453dup GRCh38
NC_000004.11:g.55991620dup , CM000666.1:g.55991620dup GRCh37
NC_000004.10:g.55686377dup NCBI36
NG_012004.1:g.5143dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-160dup MANE Select ENSP00000263923.4:n.-160dup
ENST00000263923.4:c.-160dup ENSP00000263923.4:n.-160dup
NM_002253.2:c.-160dup NP_002244.1:n.-160dup
NM_002253.3:c.-160dup NP_002244.1:n.-160dup
NM_002253.4:c.-160dup MANE Select NP_002244.1:n.-160dup
Search 100 bp 5'
Search 100 bp 3'