Canonical Allele Identifier: CA2676966982

Gene: FLT4

Linked Data

• gnomAD v4: 5-180602496-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180602496G>A , CM000667.2:g.180602496G>A	GRCh38
NC_000005.9:g.180029496G>A , CM000667.1:g.180029496G>A	GRCh37
NC_000005.8:g.179962102G>A	NCBI36
NG_011536.1:g.52129C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.*696C>T MANE Select	ENSP00000261937.6:n.*696C>T
ENST00000261937.10:c.*696C>T	ENSP00000261937.6:n.*696C>T
NM_182925.4:c.*696C>T	NP_891555.2:n.*696C>T
XM_011534477.1:c.*696C>T	XP_011532779.1:n.*696C>T
XM_011534478.1:c.*696C>T	XP_011532780.1:n.*696C>T
XM_011534482.1:c.*696C>T	XP_011532784.1:n.*696C>T
XM_011534483.1:c.*696C>T	XP_011532785.1:n.*696C>T
XM_011534484.1:c.*696C>T	XP_011532786.1:n.*696C>T
XM_011534478.3:c.*696C>T	XP_011532780.1:n.*696C>T
XM_011534484.2:c.*696C>T	XP_011532786.1:n.*696C>T
XM_017009263.1:c.*934C>T	XP_016864752.1:n.*934C>T
XM_017009268.1:c.*696C>T	XP_016864757.1:n.*696C>T
XR_001742050.2:n.5278C>T
NM_182925.5:c.*696C>T MANE Select	NP_891555.2:n.*696C>T