Canonical Allele Identifier: CA2676967654

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603290-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603290_180603291insT , CM000667.2:g.180603290_180603291insT	GRCh38
NC_000005.9:g.180030290_180030291insT , CM000667.1:g.180030290_180030291insT	GRCh37
NC_000005.8:g.179962896_179962897insT	NCBI36
NG_011536.1:g.51334_51335insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3993_3994insA MANE Select	ENSP00000261937.6:p.Phe1332IlefsTer?
ENST00000261937.10:c.3993_3994insA	ENSP00000261937.6:p.Phe1332IlefsTer?
ENST00000502603.5:n.693_694insA
NM_182925.4:c.3993_3994insA	NP_891555.2:p.Phe1332IlefsTer?
XM_011534477.1:c.4242_4243insA	XP_011532779.1:p.Phe1415IlefsTer?
XM_011534478.1:c.4224_4225insA	XP_011532780.1:p.Phe1409IlefsTer?
XM_011534482.1:c.4011_4012insA	XP_011532784.1:p.Phe1338IlefsTer?
XM_011534483.1:c.3933_3934insA	XP_011532785.1:p.Phe1312IlefsTer?
XM_011534484.1:c.3534_3535insA	XP_011532786.1:p.Phe1179IlefsTer?
XR_941095.1:n.4279_4280insA
XM_011534478.3:c.4224_4225insA	XP_011532780.1:p.Phe1409IlefsTer?
XM_011534484.2:c.3534_3535insA	XP_011532786.1:p.Phe1179IlefsTer?
XM_017009263.1:c.*139_*140insA	XP_016864752.1:n.*139_*140insA
XM_017009268.1:c.3915_3916insA	XP_016864757.1:p.Phe1306IlefsTer?
XR_001742050.2:n.4483_4484insA
NM_182925.5:c.3993_3994insA MANE Select	NP_891555.2:p.Phe1332IlefsTer?