Canonical Allele Identifier: CA2924828

Gene: KDR

Linked Data

• dbSNP Id: rs151317075
• ExAC: 4:55976857 G / C
• gnomAD v2: 4-55976857-G-C
• gnomAD v3: 4-55110690-G-C
• gnomAD v4: 4-55110690-G-C
• MyVariant Identifiers: chr4:g.55976857G>C (hg19) ; chr4:g.55110690G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55110690G>C , CM000666.2:g.55110690G>C	GRCh38
NC_000004.11:g.55976857G>C , CM000666.1:g.55976857G>C	GRCh37
NC_000004.10:g.55671614G>C	NCBI36
NG_012004.1:g.19906C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.1055C>G MANE Select	ENSP00000263923.4:p.Ala352Gly
ENST00000647068.1:n.1068C>G
ENST00000263923.4:c.1055C>G	ENSP00000263923.4:p.Ala352Gly
ENST00000512566.1:n.1055C>G
NM_002253.2:c.1055C>G	NP_002244.1:p.Ala352Gly
NM_002253.3:c.1055C>G	NP_002244.1:p.Ala352Gly
NM_002253.4:c.1055C>G MANE Select	NP_002244.1:p.Ala352Gly