Canonical Allele Identifier: CA96884307
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs778350886
gnomAD v2: 4-55957863-C-CA
gnomAD v3: 4-55091696-C-CA
gnomAD v4: 4-55091696-C-CA
MyVariant Identifiers: chr4:g.55957864_55957865insA (hg19) chr4:g.55957863_55957864insA (hg19) chr4:g.55091697_55091698insA (hg38) chr4:g.55091696_55091697insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091705dup , CM000666.2:g.55091705dup GRCh38
NC_000004.11:g.55957872dup , CM000666.1:g.55957872dup GRCh37
NC_000004.10:g.55652629dup NCBI36
NG_012004.1:g.38899dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+920dup MANE Select ENSP00000263923.4:n.3069+920dup
ENST00000647068.1:n.3082+920dup
ENST00000263923.4:c.3069+920dup ENSP00000263923.4:n.3069+920dup
NM_002253.2:c.3069+920dup NP_002244.1:n.3069+920dup
NM_002253.3:c.3069+920dup NP_002244.1:n.3069+920dup
NM_002253.4:c.3069+920dup MANE Select NP_002244.1:n.3069+920dup
Search 100 bp 5'
Search 100 bp 3'