Canonical Allele Identifier: CA362496127

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030343T>C (hg19) ; chr5:g.180603343T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603343T>C , CM000667.2:g.180603343T>C	GRCh38
NC_000005.9:g.180030343T>C , CM000667.1:g.180030343T>C	GRCh37
NC_000005.8:g.179962949T>C	NCBI36
NG_011536.1:g.51282A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3941A>G MANE Select	ENSP00000261937.6:p.Asp1314Gly
ENST00000261937.10:c.3941A>G	ENSP00000261937.6:p.Asp1314Gly
ENST00000502603.5:n.641A>G
NM_182925.4:c.3941A>G	NP_891555.2:p.Asp1314Gly
XM_011534477.1:c.4190A>G	XP_011532779.1:p.Asp1397Gly
XM_011534478.1:c.4172A>G	XP_011532780.1:p.Asp1391Gly
XM_011534479.1:c.*87A>G	XP_011532781.1:n.*87A>G
XM_011534482.1:c.3959A>G	XP_011532784.1:p.Asp1320Gly
XM_011534483.1:c.3881A>G	XP_011532785.1:p.Asp1294Gly
XM_011534484.1:c.3482A>G	XP_011532786.1:p.Asp1161Gly
XR_941095.1:n.4227A>G
XM_011534478.3:c.4172A>G	XP_011532780.1:p.Asp1391Gly
XM_011534484.2:c.3482A>G	XP_011532786.1:p.Asp1161Gly
XM_017009263.1:c.*87A>G	XP_016864752.1:n.*87A>G
XM_017009268.1:c.3863A>G	XP_016864757.1:p.Asp1288Gly
XR_001742050.2:n.4431A>G
NM_182925.5:c.3941A>G MANE Select	NP_891555.2:p.Asp1314Gly