Canonical Allele Identifier: CA796397742
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1453820037
gnomAD v3: 4-55112695-A-AT
gnomAD v4: 4-55112695-A-AT
MyVariant Identifiers: chr4:g.55978862_55978863insT (hg19) chr4:g.55112695_55112696insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112701dup , CM000666.2:g.55112701dup GRCh38
NC_000004.11:g.55978868dup , CM000666.1:g.55978868dup GRCh37
NC_000004.10:g.55673625dup NCBI36
NG_012004.1:g.17900dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.976+608dup MANE Select ENSP00000263923.4:n.976+608dup
ENST00000647068.1:n.989+608dup
ENST00000263923.4:c.976+608dup ENSP00000263923.4:n.976+608dup
ENST00000512566.1:n.976+608dup
NM_002253.2:c.976+608dup NP_002244.1:n.976+608dup
NM_002253.3:c.976+608dup NP_002244.1:n.976+608dup
NM_002253.4:c.976+608dup MANE Select NP_002244.1:n.976+608dup
Search 100 bp 5'
Search 100 bp 3'