Canonical Allele Identifier: CA133194145

Gene: FLT4

Linked Data

• dbSNP Id: rs777549987
• gnomAD v2: 5-180030508-T-TA
• gnomAD v3: 5-180603508-T-TA
• gnomAD v4: 5-180603508-T-TA
• MyVariant Identifiers: chr5:g.180030508_180030509insA (hg19) ; chr5:g.180603508_180603509insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603509dup , CM000667.2:g.180603509dup	GRCh38
NC_000005.9:g.180030509dup , CM000667.1:g.180030509dup	GRCh37
NC_000005.8:g.179963115dup	NCBI36
NG_011536.1:g.51116dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3894-119dup MANE Select	ENSP00000261937.6:n.3894-119dup
ENST00000261937.10:c.3894-119dup	ENSP00000261937.6:n.3894-119dup
ENST00000502603.5:n.594-119dup
NM_182925.4:c.3894-119dup	NP_891555.2:n.3894-119dup
XM_011534477.1:c.4143-119dup	XP_011532779.1:n.4143-119dup
XM_011534478.1:c.4125-119dup	XP_011532780.1:n.4125-119dup
XM_011534479.1:c.*40-119dup	XP_011532781.1:n.*40-119dup
XM_011534482.1:c.3912-119dup	XP_011532784.1:n.3912-119dup
XM_011534483.1:c.3834-119dup	XP_011532785.1:n.3834-119dup
XM_011534484.1:c.3435-119dup	XP_011532786.1:n.3435-119dup
XR_941095.1:n.4180-119dup
XM_011534478.3:c.4125-119dup	XP_011532780.1:n.4125-119dup
XM_011534484.2:c.3435-119dup	XP_011532786.1:n.3435-119dup
XM_017009263.1:c.*40-119dup	XP_016864752.1:n.*40-119dup
XM_017009268.1:c.3816-119dup	XP_016864757.1:n.3816-119dup
XR_001742050.2:n.4384-119dup
NM_182925.5:c.3894-119dup MANE Select	NP_891555.2:n.3894-119dup