Canonical Allele Identifier: CA2676967655

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603310-CCCCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603312_180603315del , CM000667.2:g.180603312_180603315del	GRCh38
NC_000005.9:g.180030312_180030315del , CM000667.1:g.180030312_180030315del	GRCh37
NC_000005.8:g.179962918_179962921del	NCBI36
NG_011536.1:g.51311_51314del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3970_3973del MANE Select	ENSP00000261937.6:p.Arg1324GlyfsTer?
ENST00000261937.10:c.3970_3973del	ENSP00000261937.6:p.Arg1324GlyfsTer?
ENST00000502603.5:n.670_673del
NM_182925.4:c.3970_3973del	NP_891555.2:p.Arg1324GlyfsTer?
XM_011534477.1:c.4219_4222del	XP_011532779.1:p.Arg1407GlyfsTer?
XM_011534478.1:c.4201_4204del	XP_011532780.1:p.Arg1401GlyfsTer?
XM_011534479.1:c.*116_*119del	XP_011532781.1:n.*116_*119del
XM_011534482.1:c.3988_3991del	XP_011532784.1:p.Arg1330GlyfsTer?
XM_011534483.1:c.3910_3913del	XP_011532785.1:p.Arg1304GlyfsTer?
XM_011534484.1:c.3511_3514del	XP_011532786.1:p.Arg1171GlyfsTer?
XR_941095.1:n.4256_4259del
XM_011534478.3:c.4201_4204del	XP_011532780.1:p.Arg1401GlyfsTer?
XM_011534484.2:c.3511_3514del	XP_011532786.1:p.Arg1171GlyfsTer?
XM_017009263.1:c.*116_*119del	XP_016864752.1:n.*116_*119del
XM_017009268.1:c.3892_3895del	XP_016864757.1:p.Arg1298GlyfsTer?
XR_001742050.2:n.4460_4463del
NM_182925.5:c.3970_3973del MANE Select	NP_891555.2:p.Arg1324GlyfsTer?