Canonical Allele Identifier: CA362495874

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030293C>G (hg19) ; chr5:g.180603293C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603293C>G , CM000667.2:g.180603293C>G	GRCh38
NC_000005.9:g.180030293C>G , CM000667.1:g.180030293C>G	GRCh37
NC_000005.8:g.179962899C>G	NCBI36
NG_011536.1:g.51332G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3991G>C MANE Select	ENSP00000261937.6:p.Val1331Leu
ENST00000261937.10:c.3991G>C	ENSP00000261937.6:p.Val1331Leu
ENST00000502603.5:n.691G>C
NM_182925.4:c.3991G>C	NP_891555.2:p.Val1331Leu
XM_011534477.1:c.4240G>C	XP_011532779.1:p.Val1414Leu
XM_011534478.1:c.4222G>C	XP_011532780.1:p.Val1408Leu
XM_011534482.1:c.4009G>C	XP_011532784.1:p.Val1337Leu
XM_011534483.1:c.3931G>C	XP_011532785.1:p.Val1311Leu
XM_011534484.1:c.3532G>C	XP_011532786.1:p.Val1178Leu
XR_941095.1:n.4277G>C
XM_011534478.3:c.4222G>C	XP_011532780.1:p.Val1408Leu
XM_011534484.2:c.3532G>C	XP_011532786.1:p.Val1178Leu
XM_017009263.1:c.*137G>C	XP_016864752.1:n.*137G>C
XM_017009268.1:c.3913G>C	XP_016864757.1:p.Val1305Leu
XR_001742050.2:n.4481G>C
NM_182925.5:c.3991G>C MANE Select	NP_891555.2:p.Val1331Leu