Canonical Allele Identifier: CA1604713991

Gene: FLT4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603410_180603412delinsGGT , CM000667.2:g.180603410_180603412delinsGGT	GRCh38
NC_000005.9:g.180030410_180030412delinsGGT , CM000667.1:g.180030410_180030412delinsGGT	GRCh37
NC_000005.8:g.179963016_179963018delinsGGT	NCBI36
NG_011536.1:g.51213_51215delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3894-22_3894-20delinsACC MANE Select	ENSP00000261937.6:n.3894-22_3894-20delinsACC
ENST00000261937.10:c.3894-22_3894-20delinsACC	ENSP00000261937.6:n.3894-22_3894-20delinsACC
ENST00000502603.5:n.594-22_594-20delinsACC
NM_182925.4:c.3894-22_3894-20delinsACC	NP_891555.2:n.3894-22_3894-20delinsACC
XM_011534477.1:c.4143-22_4143-20delinsACC	XP_011532779.1:n.4143-22_4143-20delinsACC
XM_011534478.1:c.4125-22_4125-20delinsACC	XP_011532780.1:n.4125-22_4125-20delinsACC
XM_011534479.1:c.*40-22_*40-20delinsACC	XP_011532781.1:n.*40-22_*40-20delinsACC
XM_011534482.1:c.3912-22_3912-20delinsACC	XP_011532784.1:n.3912-22_3912-20delinsACC
XM_011534483.1:c.3834-22_3834-20delinsACC	XP_011532785.1:n.3834-22_3834-20delinsACC
XM_011534484.1:c.3435-22_3435-20delinsACC	XP_011532786.1:n.3435-22_3435-20delinsACC
XR_941095.1:n.4180-22_4180-20delinsACC
XM_011534478.3:c.4125-22_4125-20delinsACC	XP_011532780.1:n.4125-22_4125-20delinsACC
XM_011534484.2:c.3435-22_3435-20delinsACC	XP_011532786.1:n.3435-22_3435-20delinsACC
XM_017009263.1:c.*40-22_*40-20delinsACC	XP_016864752.1:n.*40-22_*40-20delinsACC
XM_017009268.1:c.3816-22_3816-20delinsACC	XP_016864757.1:n.3816-22_3816-20delinsACC
XR_001742050.2:n.4384-22_4384-20delinsACC
NM_182925.5:c.3894-22_3894-20delinsACC MANE Select	NP_891555.2:n.3894-22_3894-20delinsACC