Canonical Allele Identifier: CA356913258
Gene: KDR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110564T>A , CM000666.2:g.55110564T>A GRCh38
NC_000004.11:g.55976731T>A , CM000666.1:g.55976731T>A GRCh37
NC_000004.10:g.55671488T>A NCBI36
NG_012004.1:g.20032A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1094A>T MANE Select ENSP00000263923.4:p.Tyr365Phe
ENST00000647068.1:n.1107A>T
ENST00000263923.4:c.1094A>T ENSP00000263923.4:p.Tyr365Phe
ENST00000512566.1:n.1094A>T
NM_002253.2:c.1094A>T NP_002244.1:p.Tyr365Phe
NM_002253.3:c.1094A>T NP_002244.1:p.Tyr365Phe
NM_002253.4:c.1094A>T MANE Select NP_002244.1:p.Tyr365Phe