Canonical Allele Identifier: CA448099092

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030339G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603339G>T , CM000667.2:g.180603339G>T	GRCh38
NC_000005.9:g.180030339G>T , CM000667.1:g.180030339G>T	GRCh37
NC_000005.8:g.179962945G>T	NCBI36
NG_011536.1:g.51286C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3945C>A MANE Select	ENSP00000261937.6:p.Ser1315=
ENST00000261937.10:c.3945C>A	ENSP00000261937.6:p.Ser1315=
ENST00000502603.5:n.645C>A
NM_182925.4:c.3945C>A	NP_891555.2:p.Ser1315=
XM_011534477.1:c.4194C>A	XP_011532779.1:p.Ser1398=
XM_011534478.1:c.4176C>A	XP_011532780.1:p.Ser1392=
XM_011534479.1:c.*91C>A	XP_011532781.1:n.*91C>A
XM_011534482.1:c.3963C>A	XP_011532784.1:p.Ser1321=
XM_011534483.1:c.3885C>A	XP_011532785.1:p.Ser1295=
XM_011534484.1:c.3486C>A	XP_011532786.1:p.Ser1162=
XR_941095.1:n.4231C>A
XM_011534478.3:c.4176C>A	XP_011532780.1:p.Ser1392=
XM_011534484.2:c.3486C>A	XP_011532786.1:p.Ser1162=
XM_017009263.1:c.*91C>A	XP_016864752.1:n.*91C>A
XM_017009268.1:c.3867C>A	XP_016864757.1:p.Ser1289=
XR_001742050.2:n.4435C>A
NM_182925.5:c.3945C>A MANE Select	NP_891555.2:p.Ser1315=