Canonical Allele Identifier: CA133193930

Gene: FLT4

Linked Data

• dbSNP Id: rs765327561
• MyVariant Identifiers: chr5:g.180030243G>T (hg19) ; chr5:g.180603243G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603243G>T , CM000667.2:g.180603243G>T	GRCh38
NC_000005.9:g.180030243G>T , CM000667.1:g.180030243G>T	GRCh37
NC_000005.8:g.179962849G>T	NCBI36
NG_011536.1:g.51382C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4041C>A MANE Select	ENSP00000261937.6:p.Asp1347Glu
ENST00000261937.10:c.4041C>A	ENSP00000261937.6:p.Asp1347Glu
ENST00000502603.5:n.741C>A
NM_182925.4:c.4041C>A	NP_891555.2:p.Asp1347Glu
XM_011534477.1:c.4290C>A	XP_011532779.1:p.Asp1430Glu
XM_011534478.1:c.4272C>A	XP_011532780.1:p.Asp1424Glu
XM_011534482.1:c.4059C>A	XP_011532784.1:p.Asp1353Glu
XM_011534483.1:c.3981C>A	XP_011532785.1:p.Asp1327Glu
XM_011534484.1:c.3582C>A	XP_011532786.1:p.Asp1194Glu
XR_941095.1:n.4327C>A
XM_011534478.3:c.4272C>A	XP_011532780.1:p.Asp1424Glu
XM_011534484.2:c.3582C>A	XP_011532786.1:p.Asp1194Glu
XM_017009263.1:c.*187C>A	XP_016864752.1:n.*187C>A
XM_017009268.1:c.3963C>A	XP_016864757.1:p.Asp1321Glu
XR_001742050.2:n.4531C>A
NM_182925.5:c.4041C>A MANE Select	NP_891555.2:p.Asp1347Glu