Canonical Allele Identifier: CA3605572

Gene: FLT4

Linked Data

• dbSNP Id: rs199750262
• ExAC: 5:180030183 C / T
• gnomAD v2: 5-180030183-C-T
• gnomAD v3: 5-180603183-C-T
• gnomAD v4: 5-180603183-C-T
• MyVariant Identifiers: chr5:g.180030183C>T (hg19) ; chr5:g.180603183C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603183C>T , CM000667.2:g.180603183C>T	GRCh38
NC_000005.9:g.180030183C>T , CM000667.1:g.180030183C>T	GRCh37
NC_000005.8:g.179962789C>T	NCBI36
NG_011536.1:g.51442G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.*9G>A MANE Select	ENSP00000261937.6:n.*9G>A
ENST00000261937.10:c.*9G>A	ENSP00000261937.6:n.*9G>A
ENST00000502603.5:n.801G>A
NM_182925.4:c.*9G>A	NP_891555.2:n.*9G>A
XM_011534477.1:c.*9G>A	XP_011532779.1:n.*9G>A
XM_011534478.1:c.*9G>A	XP_011532780.1:n.*9G>A
XM_011534482.1:c.*9G>A	XP_011532784.1:n.*9G>A
XM_011534483.1:c.*9G>A	XP_011532785.1:n.*9G>A
XM_011534484.1:c.*9G>A	XP_011532786.1:n.*9G>A
XR_941095.1:n.4387G>A
XM_011534478.3:c.*9G>A	XP_011532780.1:n.*9G>A
XM_011534484.2:c.*9G>A	XP_011532786.1:n.*9G>A
XM_017009263.1:c.*247G>A	XP_016864752.1:n.*247G>A
XM_017009268.1:c.*9G>A	XP_016864757.1:n.*9G>A
XR_001742050.2:n.4591G>A
NM_182925.5:c.*9G>A MANE Select	NP_891555.2:n.*9G>A