Canonical Allele Identifier: CA1458911549
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096388C= , CM000666.2:g.55096388C= GRCh38
NC_000004.11:g.55962555C= , CM000666.1:g.55962555C= GRCh37
NC_000004.10:g.55657312C= NCBI36
NG_012004.1:g.34208G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-46G= MANE Select ENSP00000263923.4:n.2615-46G=
ENST00000647068.1:n.2628-46G=
ENST00000263923.4:c.2615-46G= ENSP00000263923.4:n.2615-46G=
ENST00000509309.1:n.333G=
NM_002253.2:c.2615-46G= NP_002244.1:n.2615-46G=
NM_002253.3:c.2615-46G= NP_002244.1:n.2615-46G=
NM_002253.4:c.2615-46G= MANE Select NP_002244.1:n.2615-46G=