Canonical Allele Identifier: CA448099129

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030378A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603378A>T , CM000667.2:g.180603378A>T	GRCh38
NC_000005.9:g.180030378A>T , CM000667.1:g.180030378A>T	GRCh37
NC_000005.8:g.179962984A>T	NCBI36
NG_011536.1:g.51247T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3906T>A MANE Select	ENSP00000261937.6:p.Pro1302=
ENST00000261937.10:c.3906T>A	ENSP00000261937.6:p.Pro1302=
ENST00000502603.5:n.606T>A
NM_182925.4:c.3906T>A	NP_891555.2:p.Pro1302=
XM_011534477.1:c.4155T>A	XP_011532779.1:p.Pro1385=
XM_011534478.1:c.4137T>A	XP_011532780.1:p.Pro1379=
XM_011534479.1:c.*52T>A	XP_011532781.1:n.*52T>A
XM_011534482.1:c.3924T>A	XP_011532784.1:p.Pro1308=
XM_011534483.1:c.3846T>A	XP_011532785.1:p.Pro1282=
XM_011534484.1:c.3447T>A	XP_011532786.1:p.Pro1149=
XR_941095.1:n.4192T>A
XM_011534478.3:c.4137T>A	XP_011532780.1:p.Pro1379=
XM_011534484.2:c.3447T>A	XP_011532786.1:p.Pro1149=
XM_017009263.1:c.*52T>A	XP_016864752.1:n.*52T>A
XM_017009268.1:c.3828T>A	XP_016864757.1:p.Pro1276=
XR_001742050.2:n.4396T>A
NM_182925.5:c.3906T>A MANE Select	NP_891555.2:p.Pro1302=