Canonical Allele Identifier: CA362495804

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030282G>C (hg19) ; chr5:g.180603282G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603282G>C , CM000667.2:g.180603282G>C	GRCh38
NC_000005.9:g.180030282G>C , CM000667.1:g.180030282G>C	GRCh37
NC_000005.8:g.179962888G>C	NCBI36
NG_011536.1:g.51343C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4002C>G MANE Select	ENSP00000261937.6:p.Asn1334Lys
ENST00000261937.10:c.4002C>G	ENSP00000261937.6:p.Asn1334Lys
ENST00000502603.5:n.702C>G
NM_182925.4:c.4002C>G	NP_891555.2:p.Asn1334Lys
XM_011534477.1:c.4251C>G	XP_011532779.1:p.Asn1417Lys
XM_011534478.1:c.4233C>G	XP_011532780.1:p.Asn1411Lys
XM_011534482.1:c.4020C>G	XP_011532784.1:p.Asn1340Lys
XM_011534483.1:c.3942C>G	XP_011532785.1:p.Asn1314Lys
XM_011534484.1:c.3543C>G	XP_011532786.1:p.Asn1181Lys
XR_941095.1:n.4288C>G
XM_011534478.3:c.4233C>G	XP_011532780.1:p.Asn1411Lys
XM_011534484.2:c.3543C>G	XP_011532786.1:p.Asn1181Lys
XM_017009263.1:c.*148C>G	XP_016864752.1:n.*148C>G
XM_017009268.1:c.3924C>G	XP_016864757.1:p.Asn1308Lys
XR_001742050.2:n.4492C>G
NM_182925.5:c.4002C>G MANE Select	NP_891555.2:p.Asn1334Lys