Canonical Allele Identifier: CA1458926485
Gene: KDR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55087309A= , CM000666.2:g.55087309A= GRCh38
NC_000004.11:g.55953476A= , CM000666.1:g.55953476A= GRCh37
NC_000004.10:g.55648233A= NCBI36
NG_012004.1:g.43287T=

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.3662+298T= MANE Select ENSP00000263923.4:n.3662+298T=
ENST00000647068.1:n.3675+298T=
ENST00000263923.4:c.3662+298T= ENSP00000263923.4:n.3662+298T=
NM_002253.2:c.3662+298T= NP_002244.1:n.3662+298T=
NM_002253.3:c.3662+298T= NP_002244.1:n.3662+298T=
NM_002253.4:c.3662+298T= MANE Select NP_002244.1:n.3662+298T=