Canonical Allele Identifier: CA1604714057

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603536_180603537delinsAC , CM000667.2:g.180603536_180603537delinsAC	GRCh38
NC_000005.9:g.180030536_180030537delinsAC , CM000667.1:g.180030536_180030537delinsAC	GRCh37
NC_000005.8:g.179963142_179963143delinsAC	NCBI36
NG_011536.1:g.51088_51089delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3894-147_3894-146delinsGT MANE Select	ENSP00000261937.6:n.3894-147_3894-146delinsGT
ENST00000261937.10:c.3894-147_3894-146delinsGT	ENSP00000261937.6:n.3894-147_3894-146delinsGT
ENST00000502603.5:n.594-147_594-146delinsGT
NM_182925.4:c.3894-147_3894-146delinsGT	NP_891555.2:n.3894-147_3894-146delinsGT
XM_011534477.1:c.4143-147_4143-146delinsGT	XP_011532779.1:n.4143-147_4143-146delinsGT
XM_011534478.1:c.4125-147_4125-146delinsGT	XP_011532780.1:n.4125-147_4125-146delinsGT
XM_011534479.1:c.*40-147_*40-146delinsGT	XP_011532781.1:n.*40-147_*40-146delinsGT
XM_011534482.1:c.3912-147_3912-146delinsGT	XP_011532784.1:n.3912-147_3912-146delinsGT
XM_011534483.1:c.3834-147_3834-146delinsGT	XP_011532785.1:n.3834-147_3834-146delinsGT
XM_011534484.1:c.3435-147_3435-146delinsGT	XP_011532786.1:n.3435-147_3435-146delinsGT
XR_941095.1:n.4180-147_4180-146delinsGT
XM_011534478.3:c.4125-147_4125-146delinsGT	XP_011532780.1:n.4125-147_4125-146delinsGT
XM_011534484.2:c.3435-147_3435-146delinsGT	XP_011532786.1:n.3435-147_3435-146delinsGT
XM_017009263.1:c.*40-147_*40-146delinsGT	XP_016864752.1:n.*40-147_*40-146delinsGT
XM_017009268.1:c.3816-147_3816-146delinsGT	XP_016864757.1:n.3816-147_3816-146delinsGT
XR_001742050.2:n.4384-147_4384-146delinsGT
NM_182925.5:c.3894-147_3894-146delinsGT MANE Select	NP_891555.2:n.3894-147_3894-146delinsGT