Canonical Allele Identifier: CA362495879

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030294C>A (hg19) ; chr5:g.180603294C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603294C>A , CM000667.2:g.180603294C>A	GRCh38
NC_000005.9:g.180030294C>A , CM000667.1:g.180030294C>A	GRCh37
NC_000005.8:g.179962900C>A	NCBI36
NG_011536.1:g.51331G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3990G>T MANE Select	ENSP00000261937.6:p.Gln1330His
ENST00000261937.10:c.3990G>T	ENSP00000261937.6:p.Gln1330His
ENST00000502603.5:n.690G>T
NM_182925.4:c.3990G>T	NP_891555.2:p.Gln1330His
XM_011534477.1:c.4239G>T	XP_011532779.1:p.Gln1413His
XM_011534478.1:c.4221G>T	XP_011532780.1:p.Gln1407His
XM_011534482.1:c.4008G>T	XP_011532784.1:p.Gln1336His
XM_011534483.1:c.3930G>T	XP_011532785.1:p.Gln1310His
XM_011534484.1:c.3531G>T	XP_011532786.1:p.Gln1177His
XR_941095.1:n.4276G>T
XM_011534478.3:c.4221G>T	XP_011532780.1:p.Gln1407His
XM_011534484.2:c.3531G>T	XP_011532786.1:p.Gln1177His
XM_017009263.1:c.*136G>T	XP_016864752.1:n.*136G>T
XM_017009268.1:c.3912G>T	XP_016864757.1:p.Gln1304His
XR_001742050.2:n.4480G>T
NM_182925.5:c.3990G>T MANE Select	NP_891555.2:p.Gln1330His