Canonical Allele Identifier: CA1458911608
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096446T= , CM000666.2:g.55096446T= GRCh38
NC_000004.11:g.55962613T= , CM000666.1:g.55962613T= GRCh37
NC_000004.10:g.55657370T= NCBI36
NG_012004.1:g.34150A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-104A= MANE Select ENSP00000263923.4:n.2615-104A=
ENST00000647068.1:n.2628-104A=
ENST00000263923.4:c.2615-104A= ENSP00000263923.4:n.2615-104A=
ENST00000509309.1:n.275A=
NM_002253.2:c.2615-104A= NP_002244.1:n.2615-104A=
NM_002253.3:c.2615-104A= NP_002244.1:n.2615-104A=
NM_002253.4:c.2615-104A= MANE Select NP_002244.1:n.2615-104A=