Canonical Allele Identifier: CA448098917

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603198-G-A
• MyVariant Identifiers: chr5:g.180030198G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603198G>A , CM000667.2:g.180603198G>A	GRCh38
NC_000005.9:g.180030198G>A , CM000667.1:g.180030198G>A	GRCh37
NC_000005.8:g.179962804G>A	NCBI36
NG_011536.1:g.51427C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4086C>T MANE Select	ENSP00000261937.6:p.Ser1362=
ENST00000261937.10:c.4086C>T	ENSP00000261937.6:p.Ser1362=
ENST00000502603.5:n.786C>T
NM_182925.4:c.4086C>T	NP_891555.2:p.Ser1362=
XM_011534477.1:c.4335C>T	XP_011532779.1:p.Ser1445=
XM_011534478.1:c.4317C>T	XP_011532780.1:p.Ser1439=
XM_011534482.1:c.4104C>T	XP_011532784.1:p.Ser1368=
XM_011534483.1:c.4026C>T	XP_011532785.1:p.Ser1342=
XM_011534484.1:c.3627C>T	XP_011532786.1:p.Ser1209=
XR_941095.1:n.4372C>T
XM_011534478.3:c.4317C>T	XP_011532780.1:p.Ser1439=
XM_011534484.2:c.3627C>T	XP_011532786.1:p.Ser1209=
XM_017009263.1:c.*232C>T	XP_016864752.1:n.*232C>T
XM_017009268.1:c.4008C>T	XP_016864757.1:p.Ser1336=
XR_001742050.2:n.4576C>T
NM_182925.5:c.4086C>T MANE Select	NP_891555.2:p.Ser1362=