Canonical Allele Identifier: CA1604714022

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603483_180603484delinsAG , CM000667.2:g.180603483_180603484delinsAG	GRCh38
NC_000005.9:g.180030483_180030484delinsAG , CM000667.1:g.180030483_180030484delinsAG	GRCh37
NC_000005.8:g.179963089_179963090delinsAG	NCBI36
NG_011536.1:g.51141_51142delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3894-94_3894-93delinsCT MANE Select	ENSP00000261937.6:n.3894-94_3894-93delinsCT
ENST00000261937.10:c.3894-94_3894-93delinsCT	ENSP00000261937.6:n.3894-94_3894-93delinsCT
ENST00000502603.5:n.594-94_594-93delinsCT
NM_182925.4:c.3894-94_3894-93delinsCT	NP_891555.2:n.3894-94_3894-93delinsCT
XM_011534477.1:c.4143-94_4143-93delinsCT	XP_011532779.1:n.4143-94_4143-93delinsCT
XM_011534478.1:c.4125-94_4125-93delinsCT	XP_011532780.1:n.4125-94_4125-93delinsCT
XM_011534479.1:c.*40-94_*40-93delinsCT	XP_011532781.1:n.*40-94_*40-93delinsCT
XM_011534482.1:c.3912-94_3912-93delinsCT	XP_011532784.1:n.3912-94_3912-93delinsCT
XM_011534483.1:c.3834-94_3834-93delinsCT	XP_011532785.1:n.3834-94_3834-93delinsCT
XM_011534484.1:c.3435-94_3435-93delinsCT	XP_011532786.1:n.3435-94_3435-93delinsCT
XR_941095.1:n.4180-94_4180-93delinsCT
XM_011534478.3:c.4125-94_4125-93delinsCT	XP_011532780.1:n.4125-94_4125-93delinsCT
XM_011534484.2:c.3435-94_3435-93delinsCT	XP_011532786.1:n.3435-94_3435-93delinsCT
XM_017009263.1:c.*40-94_*40-93delinsCT	XP_016864752.1:n.*40-94_*40-93delinsCT
XM_017009268.1:c.3816-94_3816-93delinsCT	XP_016864757.1:n.3816-94_3816-93delinsCT
XR_001742050.2:n.4384-94_4384-93delinsCT
NM_182925.5:c.3894-94_3894-93delinsCT MANE Select	NP_891555.2:n.3894-94_3894-93delinsCT