Canonical Allele Identifier: CA2676967740

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603406-AGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603411_180603413del , CM000667.2:g.180603411_180603413del	GRCh38
NC_000005.9:g.180030411_180030413del , CM000667.1:g.180030411_180030413del	GRCh37
NC_000005.8:g.179963017_179963019del	NCBI36
NG_011536.1:g.51216_51218del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3894-19_3894-17del MANE Select	ENSP00000261937.6:n.3894-19_3894-17del
ENST00000261937.10:c.3894-19_3894-17del	ENSP00000261937.6:n.3894-19_3894-17del
ENST00000502603.5:n.594-19_594-17del
NM_182925.4:c.3894-19_3894-17del	NP_891555.2:n.3894-19_3894-17del
XM_011534477.1:c.4143-19_4143-17del	XP_011532779.1:n.4143-19_4143-17del
XM_011534478.1:c.4125-19_4125-17del	XP_011532780.1:n.4125-19_4125-17del
XM_011534479.1:c.*40-19_*40-17del	XP_011532781.1:n.*40-19_*40-17del
XM_011534482.1:c.3912-19_3912-17del	XP_011532784.1:n.3912-19_3912-17del
XM_011534483.1:c.3834-19_3834-17del	XP_011532785.1:n.3834-19_3834-17del
XM_011534484.1:c.3435-19_3435-17del	XP_011532786.1:n.3435-19_3435-17del
XR_941095.1:n.4180-19_4180-17del
XM_011534478.3:c.4125-19_4125-17del	XP_011532780.1:n.4125-19_4125-17del
XM_011534484.2:c.3435-19_3435-17del	XP_011532786.1:n.3435-19_3435-17del
XM_017009263.1:c.*40-19_*40-17del	XP_016864752.1:n.*40-19_*40-17del
XM_017009268.1:c.3816-19_3816-17del	XP_016864757.1:n.3816-19_3816-17del
XR_001742050.2:n.4384-19_4384-17del
NM_182925.5:c.3894-19_3894-17del MANE Select	NP_891555.2:n.3894-19_3894-17del