Canonical Allele Identifier: CA362496181

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603352-G-A
• MyVariant Identifiers: chr5:g.180030352G>A (hg19) ; chr5:g.180603352G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603352G>A , CM000667.2:g.180603352G>A	GRCh38
NC_000005.9:g.180030352G>A , CM000667.1:g.180030352G>A	GRCh37
NC_000005.8:g.179962958G>A	NCBI36
NG_011536.1:g.51273C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3932C>T MANE Select	ENSP00000261937.6:p.Ala1311Val
ENST00000261937.10:c.3932C>T	ENSP00000261937.6:p.Ala1311Val
ENST00000502603.5:n.632C>T
NM_182925.4:c.3932C>T	NP_891555.2:p.Ala1311Val
XM_011534477.1:c.4181C>T	XP_011532779.1:p.Ala1394Val
XM_011534478.1:c.4163C>T	XP_011532780.1:p.Ala1388Val
XM_011534479.1:c.*78C>T	XP_011532781.1:n.*78C>T
XM_011534482.1:c.3950C>T	XP_011532784.1:p.Ala1317Val
XM_011534483.1:c.3872C>T	XP_011532785.1:p.Ala1291Val
XM_011534484.1:c.3473C>T	XP_011532786.1:p.Ala1158Val
XR_941095.1:n.4218C>T
XM_011534478.3:c.4163C>T	XP_011532780.1:p.Ala1388Val
XM_011534484.2:c.3473C>T	XP_011532786.1:p.Ala1158Val
XM_017009263.1:c.*78C>T	XP_016864752.1:n.*78C>T
XM_017009268.1:c.3854C>T	XP_016864757.1:p.Ala1285Val
XR_001742050.2:n.4422C>T
NM_182925.5:c.3932C>T MANE Select	NP_891555.2:p.Ala1311Val