Canonical Allele Identifier: CA1458911644
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096511T= , CM000666.2:g.55096511T= GRCh38
NC_000004.11:g.55962678T= , CM000666.1:g.55962678T= GRCh37
NC_000004.10:g.55657435T= NCBI36
NG_012004.1:g.34085A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-169A= MANE Select ENSP00000263923.4:n.2615-169A=
ENST00000647068.1:n.2628-169A=
ENST00000263923.4:c.2615-169A= ENSP00000263923.4:n.2615-169A=
ENST00000509309.1:n.210A=
NM_002253.2:c.2615-169A= NP_002244.1:n.2615-169A=
NM_002253.3:c.2615-169A= NP_002244.1:n.2615-169A=
NM_002253.4:c.2615-169A= MANE Select NP_002244.1:n.2615-169A=