Canonical Allele Identifier: CA1062704636
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1720019095
gnomAD v3: 4-55091544-TG-T
gnomAD v4: 4-55091544-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091547del , CM000666.2:g.55091547del GRCh38
NC_000004.11:g.55957714del , CM000666.1:g.55957714del GRCh37
NC_000004.10:g.55652471del NCBI36
NG_012004.1:g.39051del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+1072del MANE Select ENSP00000263923.4:n.3069+1072del
ENST00000647068.1:n.3082+1072del
ENST00000263923.4:c.3069+1072del ENSP00000263923.4:n.3069+1072del
NM_002253.2:c.3069+1072del NP_002244.1:n.3069+1072del
NM_002253.3:c.3069+1072del NP_002244.1:n.3069+1072del
NM_002253.4:c.3069+1072del MANE Select NP_002244.1:n.3069+1072del
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