Canonical Allele Identifier: CA362498032

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180036982C>A (hg19) ; chr5:g.180609982C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609982C>A , CM000667.2:g.180609982C>A	GRCh38
NC_000005.9:g.180036982C>A , CM000667.1:g.180036982C>A	GRCh37
NC_000005.8:g.179969588C>A	NCBI36
NG_011536.1:g.44643G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3730G>T MANE Select	ENSP00000261937.6:p.Ala1244Ser
ENST00000261937.10:c.3730G>T	ENSP00000261937.6:p.Ala1244Ser
ENST00000393347.7:c.3730G>T	ENSP00000377016.3:p.Ala1244Ser
ENST00000502603.5:n.430G>T
ENST00000502649.5:c.3730G>T	ENSP00000426057.1:p.Ala1244Ser
ENST00000507059.5:n.4080G>T
ENST00000619105.4:c.*2673G>T	ENSP00000481134.1:n.*2673G>T
NM_002020.4:c.3730G>T	NP_002011.2:p.Ala1244Ser
NM_182925.4:c.3730G>T	NP_891555.2:p.Ala1244Ser
XM_011534477.1:c.3979G>T	XP_011532779.1:p.Ala1327Ser
XM_011534478.1:c.3961G>T	XP_011532780.1:p.Ala1321Ser
XM_011534479.1:c.3979G>T	XP_011532781.1:p.Ala1327Ser
XM_011534480.1:c.3979G>T	XP_011532782.1:p.Ala1327Ser
XM_011534481.1:c.3979G>T	XP_011532783.1:p.Ala1327Ser
XM_011534482.1:c.3748G>T	XP_011532784.1:p.Ala1250Ser
XM_011534483.1:c.3670G>T	XP_011532785.1:p.Ala1224Ser
XM_011534484.1:c.3271G>T	XP_011532786.1:p.Ala1091Ser
XR_941095.1:n.4016G>T
NM_001354989.1:c.3730G>T	NP_001341918.1:p.Ala1244Ser
XM_011534478.3:c.3961G>T	XP_011532780.1:p.Ala1321Ser
XM_011534484.2:c.3271G>T	XP_011532786.1:p.Ala1091Ser
XM_017009263.1:c.3961G>T	XP_016864752.1:p.Ala1321Ser
XM_017009264.2:c.3961G>T	XP_016864753.1:p.Ala1321Ser
XM_017009265.1:c.3961G>T	XP_016864754.1:p.Ala1321Ser
XM_017009266.1:c.3961G>T	XP_016864755.1:p.Ala1321Ser
XM_017009267.2:c.3961G>T	XP_016864756.1:p.Ala1321Ser
XM_017009268.1:c.3652G>T	XP_016864757.1:p.Ala1218Ser
XR_001742050.2:n.4220G>T
NM_182925.5:c.3730G>T MANE Select	NP_891555.2:p.Ala1244Ser
NM_001354989.2:c.3730G>T	NP_001341918.1:p.Ala1244Ser
NM_002020.5:c.3730G>T	NP_002011.2:p.Ala1244Ser