Canonical Allele Identifier: CA362496236

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030362C>A (hg19) ; chr5:g.180603362C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603362C>A , CM000667.2:g.180603362C>A	GRCh38
NC_000005.9:g.180030362C>A , CM000667.1:g.180030362C>A	GRCh37
NC_000005.8:g.179962968C>A	NCBI36
NG_011536.1:g.51263G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3922G>T MANE Select	ENSP00000261937.6:p.Val1308Leu
ENST00000261937.10:c.3922G>T	ENSP00000261937.6:p.Val1308Leu
ENST00000502603.5:n.622G>T
NM_182925.4:c.3922G>T	NP_891555.2:p.Val1308Leu
XM_011534477.1:c.4171G>T	XP_011532779.1:p.Val1391Leu
XM_011534478.1:c.4153G>T	XP_011532780.1:p.Val1385Leu
XM_011534479.1:c.*68G>T	XP_011532781.1:n.*68G>T
XM_011534482.1:c.3940G>T	XP_011532784.1:p.Val1314Leu
XM_011534483.1:c.3862G>T	XP_011532785.1:p.Val1288Leu
XM_011534484.1:c.3463G>T	XP_011532786.1:p.Val1155Leu
XR_941095.1:n.4208G>T
XM_011534478.3:c.4153G>T	XP_011532780.1:p.Val1385Leu
XM_011534484.2:c.3463G>T	XP_011532786.1:p.Val1155Leu
XM_017009263.1:c.*68G>T	XP_016864752.1:n.*68G>T
XM_017009268.1:c.3844G>T	XP_016864757.1:p.Val1282Leu
XR_001742050.2:n.4412G>T
NM_182925.5:c.3922G>T MANE Select	NP_891555.2:p.Val1308Leu