Canonical Allele Identifier: CA362496370

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030386T>A (hg19) ; chr5:g.180603386T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603386T>A , CM000667.2:g.180603386T>A	GRCh38
NC_000005.9:g.180030386T>A , CM000667.1:g.180030386T>A	GRCh37
NC_000005.8:g.179962992T>A	NCBI36
NG_011536.1:g.51239A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3898A>T MANE Select	ENSP00000261937.6:p.Lys1300Ter
ENST00000261937.10:c.3898A>T	ENSP00000261937.6:p.Lys1300Ter
ENST00000502603.5:n.598A>T
NM_182925.4:c.3898A>T	NP_891555.2:p.Lys1300Ter
XM_011534477.1:c.4147A>T	XP_011532779.1:p.Lys1383Ter
XM_011534478.1:c.4129A>T	XP_011532780.1:p.Lys1377Ter
XM_011534479.1:c.*44A>T	XP_011532781.1:n.*44A>T
XM_011534482.1:c.3916A>T	XP_011532784.1:p.Lys1306Ter
XM_011534483.1:c.3838A>T	XP_011532785.1:p.Lys1280Ter
XM_011534484.1:c.3439A>T	XP_011532786.1:p.Lys1147Ter
XR_941095.1:n.4184A>T
XM_011534478.3:c.4129A>T	XP_011532780.1:p.Lys1377Ter
XM_011534484.2:c.3439A>T	XP_011532786.1:p.Lys1147Ter
XM_017009263.1:c.*44A>T	XP_016864752.1:n.*44A>T
XM_017009268.1:c.3820A>T	XP_016864757.1:p.Lys1274Ter
XR_001742050.2:n.4388A>T
NM_182925.5:c.3898A>T MANE Select	NP_891555.2:p.Lys1300Ter