Canonical Allele Identifier: CA1458933534
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112741G= , CM000666.2:g.55112741G= GRCh38
NC_000004.11:g.55978908G= , CM000666.1:g.55978908G= GRCh37
NC_000004.10:g.55673665G= NCBI36
NG_012004.1:g.17855C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.976+563C= MANE Select ENSP00000263923.4:n.976+563C=
ENST00000647068.1:n.989+563C=
ENST00000263923.4:c.976+563C= ENSP00000263923.4:n.976+563C=
ENST00000512566.1:n.976+563C=
NM_002253.2:c.976+563C= NP_002244.1:n.976+563C=
NM_002253.3:c.976+563C= NP_002244.1:n.976+563C=
NM_002253.4:c.976+563C= MANE Select NP_002244.1:n.976+563C=