Canonical Allele Identifier: CA448102984

Gene: FLT4

Linked Data

• gnomAD v4: 5-180614087-G-C
• MyVariant Identifiers: chr5:g.180041087G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180614087G>C , CM000667.2:g.180614087G>C	GRCh38
NC_000005.9:g.180041087G>C , CM000667.1:g.180041087G>C	GRCh37
NC_000005.8:g.179973693G>C	NCBI36
NG_011536.1:g.40538C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3312C>G MANE Select	ENSP00000261937.6:p.Leu1104=
ENST00000261937.10:c.3312C>G	ENSP00000261937.6:p.Leu1104=
ENST00000393347.7:c.3312C>G	ENSP00000377016.3:p.Leu1104=
ENST00000502649.5:c.3312C>G	ENSP00000426057.1:p.Leu1104=
ENST00000507059.5:n.2705C>G
ENST00000512795.1:c.426C>G	ENSP00000421535.1:p.Leu142=
ENST00000514810.1:n.679C>G
ENST00000619105.4:c.*2255C>G	ENSP00000481134.1:n.*2255C>G
NM_002020.4:c.3312C>G	NP_002011.2:p.Leu1104=
NM_182925.4:c.3312C>G	NP_891555.2:p.Leu1104=
XM_011534477.1:c.3561C>G	XP_011532779.1:p.Leu1187=
XM_011534478.1:c.3543C>G	XP_011532780.1:p.Leu1181=
XM_011534479.1:c.3561C>G	XP_011532781.1:p.Leu1187=
XM_011534480.1:c.3561C>G	XP_011532782.1:p.Leu1187=
XM_011534481.1:c.3561C>G	XP_011532783.1:p.Leu1187=
XM_011534482.1:c.3330C>G	XP_011532784.1:p.Leu1110=
XM_011534483.1:c.3252C>G	XP_011532785.1:p.Leu1084=
XM_011534484.1:c.2853C>G	XP_011532786.1:p.Leu951=
XR_941095.1:n.3573C>G
NM_001354989.1:c.3312C>G	NP_001341918.1:p.Leu1104=
XM_011534478.3:c.3543C>G	XP_011532780.1:p.Leu1181=
XM_011534484.2:c.2853C>G	XP_011532786.1:p.Leu951=
XM_017009263.1:c.3543C>G	XP_016864752.1:p.Leu1181=
XM_017009264.2:c.3543C>G	XP_016864753.1:p.Leu1181=
XM_017009265.1:c.3543C>G	XP_016864754.1:p.Leu1181=
XM_017009266.1:c.3543C>G	XP_016864755.1:p.Leu1181=
XM_017009267.2:c.3543C>G	XP_016864756.1:p.Leu1181=
XM_017009268.1:c.3234C>G	XP_016864757.1:p.Leu1078=
XR_001742050.2:n.3777C>G
NM_182925.5:c.3312C>G MANE Select	NP_891555.2:p.Leu1104=
NM_001354989.2:c.3312C>G	NP_001341918.1:p.Leu1104=
NM_002020.5:c.3312C>G	NP_002011.2:p.Leu1104=