Canonical Allele Identifier: CA362496379

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030387A>C (hg19) ; chr5:g.180603387A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603387A>C , CM000667.2:g.180603387A>C	GRCh38
NC_000005.9:g.180030387A>C , CM000667.1:g.180030387A>C	GRCh37
NC_000005.8:g.179962993A>C	NCBI36
NG_011536.1:g.51238T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3897T>G MANE Select	ENSP00000261937.6:p.Cys1299Trp
ENST00000261937.10:c.3897T>G	ENSP00000261937.6:p.Cys1299Trp
ENST00000502603.5:n.597T>G
NM_182925.4:c.3897T>G	NP_891555.2:p.Cys1299Trp
XM_011534477.1:c.4146T>G	XP_011532779.1:p.Cys1382Trp
XM_011534478.1:c.4128T>G	XP_011532780.1:p.Cys1376Trp
XM_011534479.1:c.*43T>G	XP_011532781.1:n.*43T>G
XM_011534482.1:c.3915T>G	XP_011532784.1:p.Cys1305Trp
XM_011534483.1:c.3837T>G	XP_011532785.1:p.Cys1279Trp
XM_011534484.1:c.3438T>G	XP_011532786.1:p.Cys1146Trp
XR_941095.1:n.4183T>G
XM_011534478.3:c.4128T>G	XP_011532780.1:p.Cys1376Trp
XM_011534484.2:c.3438T>G	XP_011532786.1:p.Cys1146Trp
XM_017009263.1:c.*43T>G	XP_016864752.1:n.*43T>G
XM_017009268.1:c.3819T>G	XP_016864757.1:p.Cys1273Trp
XR_001742050.2:n.4387T>G
NM_182925.5:c.3897T>G MANE Select	NP_891555.2:p.Cys1299Trp