Canonical Allele Identifier: CA362495520

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030246C>G (hg19) ; chr5:g.180603246C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603246C>G , CM000667.2:g.180603246C>G	GRCh38
NC_000005.9:g.180030246C>G , CM000667.1:g.180030246C>G	GRCh37
NC_000005.8:g.179962852C>G	NCBI36
NG_011536.1:g.51379G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4038G>C MANE Select	ENSP00000261937.6:p.Glu1346Asp
ENST00000261937.10:c.4038G>C	ENSP00000261937.6:p.Glu1346Asp
ENST00000502603.5:n.738G>C
NM_182925.4:c.4038G>C	NP_891555.2:p.Glu1346Asp
XM_011534477.1:c.4287G>C	XP_011532779.1:p.Glu1429Asp
XM_011534478.1:c.4269G>C	XP_011532780.1:p.Glu1423Asp
XM_011534482.1:c.4056G>C	XP_011532784.1:p.Glu1352Asp
XM_011534483.1:c.3978G>C	XP_011532785.1:p.Glu1326Asp
XM_011534484.1:c.3579G>C	XP_011532786.1:p.Glu1193Asp
XR_941095.1:n.4324G>C
XM_011534478.3:c.4269G>C	XP_011532780.1:p.Glu1423Asp
XM_011534484.2:c.3579G>C	XP_011532786.1:p.Glu1193Asp
XM_017009263.1:c.*184G>C	XP_016864752.1:n.*184G>C
XM_017009268.1:c.3960G>C	XP_016864757.1:p.Glu1320Asp
XR_001742050.2:n.4528G>C
NM_182925.5:c.4038G>C MANE Select	NP_891555.2:p.Glu1346Asp