Canonical Allele Identifier: CA1458926489
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55087315C= , CM000666.2:g.55087315C= GRCh38
NC_000004.11:g.55953482C= , CM000666.1:g.55953482C= GRCh37
NC_000004.10:g.55648239C= NCBI36
NG_012004.1:g.43281G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3662+292G= MANE Select ENSP00000263923.4:n.3662+292G=
ENST00000647068.1:n.3675+292G=
ENST00000263923.4:c.3662+292G= ENSP00000263923.4:n.3662+292G=
NM_002253.2:c.3662+292G= NP_002244.1:n.3662+292G=
NM_002253.3:c.3662+292G= NP_002244.1:n.3662+292G=
NM_002253.4:c.3662+292G= MANE Select NP_002244.1:n.3662+292G=