Canonical Allele Identifier: CA362495985

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603315-C-G
• MyVariant Identifiers: chr5:g.180030315C>G (hg19) ; chr5:g.180603315C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603315C>G , CM000667.2:g.180603315C>G	GRCh38
NC_000005.9:g.180030315C>G , CM000667.1:g.180030315C>G	GRCh37
NC_000005.8:g.179962921C>G	NCBI36
NG_011536.1:g.51310G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3969G>C MANE Select	ENSP00000261937.6:p.Glu1323Asp
ENST00000261937.10:c.3969G>C	ENSP00000261937.6:p.Glu1323Asp
ENST00000502603.5:n.669G>C
NM_182925.4:c.3969G>C	NP_891555.2:p.Glu1323Asp
XM_011534477.1:c.4218G>C	XP_011532779.1:p.Glu1406Asp
XM_011534478.1:c.4200G>C	XP_011532780.1:p.Glu1400Asp
XM_011534479.1:c.*115G>C	XP_011532781.1:n.*115G>C
XM_011534482.1:c.3987G>C	XP_011532784.1:p.Glu1329Asp
XM_011534483.1:c.3909G>C	XP_011532785.1:p.Glu1303Asp
XM_011534484.1:c.3510G>C	XP_011532786.1:p.Glu1170Asp
XR_941095.1:n.4255G>C
XM_011534478.3:c.4200G>C	XP_011532780.1:p.Glu1400Asp
XM_011534484.2:c.3510G>C	XP_011532786.1:p.Glu1170Asp
XM_017009263.1:c.*115G>C	XP_016864752.1:n.*115G>C
XM_017009268.1:c.3891G>C	XP_016864757.1:p.Glu1297Asp
XR_001742050.2:n.4459G>C
NM_182925.5:c.3969G>C MANE Select	NP_891555.2:p.Glu1323Asp