Canonical Allele Identifier: CA362496367

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030385T>G (hg19) ; chr5:g.180603385T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603385T>G , CM000667.2:g.180603385T>G	GRCh38
NC_000005.9:g.180030385T>G , CM000667.1:g.180030385T>G	GRCh37
NC_000005.8:g.179962991T>G	NCBI36
NG_011536.1:g.51240A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3899A>C MANE Select	ENSP00000261937.6:p.Lys1300Thr
ENST00000261937.10:c.3899A>C	ENSP00000261937.6:p.Lys1300Thr
ENST00000502603.5:n.599A>C
NM_182925.4:c.3899A>C	NP_891555.2:p.Lys1300Thr
XM_011534477.1:c.4148A>C	XP_011532779.1:p.Lys1383Thr
XM_011534478.1:c.4130A>C	XP_011532780.1:p.Lys1377Thr
XM_011534479.1:c.*45A>C	XP_011532781.1:n.*45A>C
XM_011534482.1:c.3917A>C	XP_011532784.1:p.Lys1306Thr
XM_011534483.1:c.3839A>C	XP_011532785.1:p.Lys1280Thr
XM_011534484.1:c.3440A>C	XP_011532786.1:p.Lys1147Thr
XR_941095.1:n.4185A>C
XM_011534478.3:c.4130A>C	XP_011532780.1:p.Lys1377Thr
XM_011534484.2:c.3440A>C	XP_011532786.1:p.Lys1147Thr
XM_017009263.1:c.*45A>C	XP_016864752.1:n.*45A>C
XM_017009268.1:c.3821A>C	XP_016864757.1:p.Lys1274Thr
XR_001742050.2:n.4389A>C
NM_182925.5:c.3899A>C MANE Select	NP_891555.2:p.Lys1300Thr