Canonical Allele Identifier: CA133194062

Gene: FLT4

Linked Data

• dbSNP Id: rs200392269
• gnomAD v2: 5-180030320-G-A
• gnomAD v4: 5-180603320-G-A
• MyVariant Identifiers: chr5:g.180030320G>A (hg19) ; chr5:g.180603320G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603320G>A , CM000667.2:g.180603320G>A	GRCh38
NC_000005.9:g.180030320G>A , CM000667.1:g.180030320G>A	GRCh37
NC_000005.8:g.179962926G>A	NCBI36
NG_011536.1:g.51305C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3964C>T MANE Select	ENSP00000261937.6:p.Pro1322Ser
ENST00000261937.10:c.3964C>T	ENSP00000261937.6:p.Pro1322Ser
ENST00000502603.5:n.664C>T
NM_182925.4:c.3964C>T	NP_891555.2:p.Pro1322Ser
XM_011534477.1:c.4213C>T	XP_011532779.1:p.Pro1405Ser
XM_011534478.1:c.4195C>T	XP_011532780.1:p.Pro1399Ser
XM_011534479.1:c.*110C>T	XP_011532781.1:n.*110C>T
XM_011534482.1:c.3982C>T	XP_011532784.1:p.Pro1328Ser
XM_011534483.1:c.3904C>T	XP_011532785.1:p.Pro1302Ser
XM_011534484.1:c.3505C>T	XP_011532786.1:p.Pro1169Ser
XR_941095.1:n.4250C>T
XM_011534478.3:c.4195C>T	XP_011532780.1:p.Pro1399Ser
XM_011534484.2:c.3505C>T	XP_011532786.1:p.Pro1169Ser
XM_017009263.1:c.*110C>T	XP_016864752.1:n.*110C>T
XM_017009268.1:c.3886C>T	XP_016864757.1:p.Pro1296Ser
XR_001742050.2:n.4454C>T
NM_182925.5:c.3964C>T MANE Select	NP_891555.2:p.Pro1322Ser