Canonical Allele Identifier: CA362495372

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030211A>G (hg19) ; chr5:g.180603211A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603211A>G , CM000667.2:g.180603211A>G	GRCh38
NC_000005.9:g.180030211A>G , CM000667.1:g.180030211A>G	GRCh37
NC_000005.8:g.179962817A>G	NCBI36
NG_011536.1:g.51414T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4073T>C MANE Select	ENSP00000261937.6:p.Phe1358Ser
ENST00000261937.10:c.4073T>C	ENSP00000261937.6:p.Phe1358Ser
ENST00000502603.5:n.773T>C
NM_182925.4:c.4073T>C	NP_891555.2:p.Phe1358Ser
XM_011534477.1:c.4322T>C	XP_011532779.1:p.Phe1441Ser
XM_011534478.1:c.4304T>C	XP_011532780.1:p.Phe1435Ser
XM_011534482.1:c.4091T>C	XP_011532784.1:p.Phe1364Ser
XM_011534483.1:c.4013T>C	XP_011532785.1:p.Phe1338Ser
XM_011534484.1:c.3614T>C	XP_011532786.1:p.Phe1205Ser
XR_941095.1:n.4359T>C
XM_011534478.3:c.4304T>C	XP_011532780.1:p.Phe1435Ser
XM_011534484.2:c.3614T>C	XP_011532786.1:p.Phe1205Ser
XM_017009263.1:c.*219T>C	XP_016864752.1:n.*219T>C
XM_017009268.1:c.3995T>C	XP_016864757.1:p.Phe1332Ser
XR_001742050.2:n.4563T>C
NM_182925.5:c.4073T>C MANE Select	NP_891555.2:p.Phe1358Ser