Canonical Allele Identifier: CA2676967726

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603383-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603386del , CM000667.2:g.180603386del	GRCh38
NC_000005.9:g.180030386del , CM000667.1:g.180030386del	GRCh37
NC_000005.8:g.179962992del	NCBI36
NG_011536.1:g.51241del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3900del MANE Select	ENSP00000261937.6:p.Gly1301AspfsTer8
ENST00000261937.10:c.3900del	ENSP00000261937.6:p.Gly1301AspfsTer8
ENST00000502603.5:n.600del
NM_182925.4:c.3900del	NP_891555.2:p.Gly1301AspfsTer8
XM_011534477.1:c.4149del	XP_011532779.1:p.Gly1384AspfsTer8
XM_011534478.1:c.4131del	XP_011532780.1:p.Gly1378AspfsTer8
XM_011534479.1:c.*46del	XP_011532781.1:n.*46del
XM_011534482.1:c.3918del	XP_011532784.1:p.Gly1307AspfsTer8
XM_011534483.1:c.3840del	XP_011532785.1:p.Gly1281AspfsTer8
XM_011534484.1:c.3441del	XP_011532786.1:p.Gly1148AspfsTer8
XR_941095.1:n.4186del
XM_011534478.3:c.4131del	XP_011532780.1:p.Gly1378AspfsTer8
XM_011534484.2:c.3441del	XP_011532786.1:p.Gly1148AspfsTer8
XM_017009263.1:c.*46del	XP_016864752.1:n.*46del
XM_017009268.1:c.3822del	XP_016864757.1:p.Gly1275AspfsTer8
XR_001742050.2:n.4390del
NM_182925.5:c.3900del MANE Select	NP_891555.2:p.Gly1301AspfsTer8