Canonical Allele Identifier: CA439489586
Gene: KDR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.55991398A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125231A>T , CM000666.2:g.55125231A>T GRCh38
NC_000004.11:g.55991398A>T , CM000666.1:g.55991398A>T GRCh37
NC_000004.10:g.55686155A>T NCBI36
NG_012004.1:g.5365T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.63T>A MANE Select ENSP00000263923.4:p.Ser21=
ENST00000263923.4:c.63T>A ENSP00000263923.4:p.Ser21=
ENST00000512566.1:n.63T>A
NM_002253.2:c.63T>A NP_002244.1:p.Ser21=
NM_002253.3:c.63T>A NP_002244.1:p.Ser21=
NM_002253.4:c.63T>A MANE Select NP_002244.1:p.Ser21=