Canonical Allele Identifier: CA796419829
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1370223598
gnomAD v3: 4-55091690-GA-G
gnomAD v4: 4-55091690-GA-G
MyVariant Identifiers: chr4:g.55957858del (hg19) chr4:g.55091691del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091695del , CM000666.2:g.55091695del GRCh38
NC_000004.11:g.55957862del , CM000666.1:g.55957862del GRCh37
NC_000004.10:g.55652619del NCBI36
NG_012004.1:g.38905del

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+926del MANE Select ENSP00000263923.4:n.3069+926del
ENST00000647068.1:n.3082+926del
ENST00000263923.4:c.3069+926del ENSP00000263923.4:n.3069+926del
NM_002253.2:c.3069+926del NP_002244.1:n.3069+926del
NM_002253.3:c.3069+926del NP_002244.1:n.3069+926del
NM_002253.4:c.3069+926del MANE Select NP_002244.1:n.3069+926del
Search 100 bp 5'
Search 100 bp 3'