Canonical Allele Identifier: CA1458911667
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096553A= , CM000666.2:g.55096553A= GRCh38
NC_000004.11:g.55962720A= , CM000666.1:g.55962720A= GRCh37
NC_000004.10:g.55657477A= NCBI36
NG_012004.1:g.34043T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-211T= MANE Select ENSP00000263923.4:n.2615-211T=
ENST00000647068.1:n.2628-211T=
ENST00000263923.4:c.2615-211T= ENSP00000263923.4:n.2615-211T=
ENST00000509309.1:n.168T=
NM_002253.2:c.2615-211T= NP_002244.1:n.2615-211T=
NM_002253.3:c.2615-211T= NP_002244.1:n.2615-211T=
NM_002253.4:c.2615-211T= MANE Select NP_002244.1:n.2615-211T=