Canonical Allele Identifier: CA1458933542
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112752A= , CM000666.2:g.55112752A= GRCh38
NC_000004.11:g.55978919A= , CM000666.1:g.55978919A= GRCh37
NC_000004.10:g.55673676A= NCBI36
NG_012004.1:g.17844T=

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.976+552T= MANE Select ENSP00000263923.4:n.976+552T=
ENST00000647068.1:n.989+552T=
ENST00000263923.4:c.976+552T= ENSP00000263923.4:n.976+552T=
ENST00000512566.1:n.976+552T=
NM_002253.2:c.976+552T= NP_002244.1:n.976+552T=
NM_002253.3:c.976+552T= NP_002244.1:n.976+552T=
NM_002253.4:c.976+552T= MANE Select NP_002244.1:n.976+552T=