Canonical Allele Identifier: CA362495366

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030209T>C (hg19) ; chr5:g.180603209T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603209T>C , CM000667.2:g.180603209T>C	GRCh38
NC_000005.9:g.180030209T>C , CM000667.1:g.180030209T>C	GRCh37
NC_000005.8:g.179962815T>C	NCBI36
NG_011536.1:g.51416A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4075A>G MANE Select	ENSP00000261937.6:p.Thr1359Ala
ENST00000261937.10:c.4075A>G	ENSP00000261937.6:p.Thr1359Ala
ENST00000502603.5:n.775A>G
NM_182925.4:c.4075A>G	NP_891555.2:p.Thr1359Ala
XM_011534477.1:c.4324A>G	XP_011532779.1:p.Thr1442Ala
XM_011534478.1:c.4306A>G	XP_011532780.1:p.Thr1436Ala
XM_011534482.1:c.4093A>G	XP_011532784.1:p.Thr1365Ala
XM_011534483.1:c.4015A>G	XP_011532785.1:p.Thr1339Ala
XM_011534484.1:c.3616A>G	XP_011532786.1:p.Thr1206Ala
XR_941095.1:n.4361A>G
XM_011534478.3:c.4306A>G	XP_011532780.1:p.Thr1436Ala
XM_011534484.2:c.3616A>G	XP_011532786.1:p.Thr1206Ala
XM_017009263.1:c.*221A>G	XP_016864752.1:n.*221A>G
XM_017009268.1:c.3997A>G	XP_016864757.1:p.Thr1333Ala
XR_001742050.2:n.4565A>G
NM_182925.5:c.4075A>G MANE Select	NP_891555.2:p.Thr1359Ala