Canonical Allele Identifier: CA1458911634
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096495G= , CM000666.2:g.55096495G= GRCh38
NC_000004.11:g.55962662G= , CM000666.1:g.55962662G= GRCh37
NC_000004.10:g.55657419G= NCBI36
NG_012004.1:g.34101C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-153C= MANE Select ENSP00000263923.4:n.2615-153C=
ENST00000647068.1:n.2628-153C=
ENST00000263923.4:c.2615-153C= ENSP00000263923.4:n.2615-153C=
ENST00000509309.1:n.226C=
NM_002253.2:c.2615-153C= NP_002244.1:n.2615-153C=
NM_002253.3:c.2615-153C= NP_002244.1:n.2615-153C=
NM_002253.4:c.2615-153C= MANE Select NP_002244.1:n.2615-153C=