Canonical Allele Identifier: CA796397213

Gene: KDR

Linked Data

• dbSNP Id: rs1399446277
• MyVariant Identifiers: chr4:g.55978191_55978192insCAT (hg19) ; chr4:g.55112024_55112025insCAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55112025_55112026insATC , CM000666.2:g.55112025_55112026insATC	GRCh38
NC_000004.11:g.55978192_55978193insATC , CM000666.1:g.55978192_55978193insATC	GRCh37
NC_000004.10:g.55672949_55672950insATC	NCBI36
NG_012004.1:g.18571_18572insATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.977-1257_977-1256insATG MANE Select	ENSP00000263923.4:n.977-1257_977-1256insATG
ENST00000647068.1:n.990-1257_990-1256insATG
ENST00000263923.4:c.977-1257_977-1256insATG	ENSP00000263923.4:n.977-1257_977-1256insATG
ENST00000512566.1:n.977-1257_977-1256insATG
NM_002253.2:c.977-1257_977-1256insATG	NP_002244.1:n.977-1257_977-1256insATG
NM_002253.3:c.977-1257_977-1256insATG	NP_002244.1:n.977-1257_977-1256insATG
NM_002253.4:c.977-1257_977-1256insATG MANE Select	NP_002244.1:n.977-1257_977-1256insATG