Canonical Allele Identifier: CA362496375

Gene: FLT4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3898A>C MANE Select	ENSP00000261937.6:p.Lys1300Gln
ENST00000261937.10:c.3898A>C	ENSP00000261937.6:p.Lys1300Gln
ENST00000502603.5:n.598A>C
NM_182925.4:c.3898A>C	NP_891555.2:p.Lys1300Gln
XM_011534477.1:c.4147A>C	XP_011532779.1:p.Lys1383Gln
XM_011534478.1:c.4129A>C	XP_011532780.1:p.Lys1377Gln
XM_011534479.1:c.*44A>C	XP_011532781.1:n.*44A>C
XM_011534482.1:c.3916A>C	XP_011532784.1:p.Lys1306Gln
XM_011534483.1:c.3838A>C	XP_011532785.1:p.Lys1280Gln
XM_011534484.1:c.3439A>C	XP_011532786.1:p.Lys1147Gln
XR_941095.1:n.4184A>C
XM_011534478.3:c.4129A>C	XP_011532780.1:p.Lys1377Gln
XM_011534484.2:c.3439A>C	XP_011532786.1:p.Lys1147Gln
XM_017009263.1:c.*44A>C	XP_016864752.1:n.*44A>C
XM_017009268.1:c.3820A>C	XP_016864757.1:p.Lys1274Gln
XR_001742050.2:n.4388A>C
NM_182925.5:c.3898A>C MANE Select	NP_891555.2:p.Lys1300Gln