Canonical Allele Identifier: CA796397737

Gene: KDR

Linked Data

• dbSNP Id: rs1467013751
• gnomAD v3: 4-55112682-C-CCA
• gnomAD v4: 4-55112682-C-CCA
• MyVariant Identifiers: chr4:g.55978849_55978850insCA (hg19) ; chr4:g.55112682_55112683insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55112686_55112687dup , CM000666.2:g.55112686_55112687dup	GRCh38
NC_000004.11:g.55978853_55978854dup , CM000666.1:g.55978853_55978854dup	GRCh37
NC_000004.10:g.55673610_55673611dup	NCBI36
NG_012004.1:g.17912_17913dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.976+620_976+621dup MANE Select	ENSP00000263923.4:n.976+620_976+621dup
ENST00000647068.1:n.989+620_989+621dup
ENST00000263923.4:c.976+620_976+621dup	ENSP00000263923.4:n.976+620_976+621dup
ENST00000512566.1:n.976+620_976+621dup
NM_002253.2:c.976+620_976+621dup	NP_002244.1:n.976+620_976+621dup
NM_002253.3:c.976+620_976+621dup	NP_002244.1:n.976+620_976+621dup
NM_002253.4:c.976+620_976+621dup MANE Select	NP_002244.1:n.976+620_976+621dup