Canonical Allele Identifier: CA362495895

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603295-T-G
• MyVariant Identifiers: chr5:g.180030295T>G (hg19) ; chr5:g.180603295T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603295T>G , CM000667.2:g.180603295T>G	GRCh38
NC_000005.9:g.180030295T>G , CM000667.1:g.180030295T>G	GRCh37
NC_000005.8:g.179962901T>G	NCBI36
NG_011536.1:g.51330A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3989A>C MANE Select	ENSP00000261937.6:p.Gln1330Pro
ENST00000261937.10:c.3989A>C	ENSP00000261937.6:p.Gln1330Pro
ENST00000502603.5:n.689A>C
NM_182925.4:c.3989A>C	NP_891555.2:p.Gln1330Pro
XM_011534477.1:c.4238A>C	XP_011532779.1:p.Gln1413Pro
XM_011534478.1:c.4220A>C	XP_011532780.1:p.Gln1407Pro
XM_011534482.1:c.4007A>C	XP_011532784.1:p.Gln1336Pro
XM_011534483.1:c.3929A>C	XP_011532785.1:p.Gln1310Pro
XM_011534484.1:c.3530A>C	XP_011532786.1:p.Gln1177Pro
XR_941095.1:n.4275A>C
XM_011534478.3:c.4220A>C	XP_011532780.1:p.Gln1407Pro
XM_011534484.2:c.3530A>C	XP_011532786.1:p.Gln1177Pro
XM_017009263.1:c.*135A>C	XP_016864752.1:n.*135A>C
XM_017009268.1:c.3911A>C	XP_016864757.1:p.Gln1304Pro
XR_001742050.2:n.4479A>C
NM_182925.5:c.3989A>C MANE Select	NP_891555.2:p.Gln1330Pro