Canonical Allele Identifier: CA448099045

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030282G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603282G>A , CM000667.2:g.180603282G>A	GRCh38
NC_000005.9:g.180030282G>A , CM000667.1:g.180030282G>A	GRCh37
NC_000005.8:g.179962888G>A	NCBI36
NG_011536.1:g.51343C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4002C>T MANE Select	ENSP00000261937.6:p.Asn1334=
ENST00000261937.10:c.4002C>T	ENSP00000261937.6:p.Asn1334=
ENST00000502603.5:n.702C>T
NM_182925.4:c.4002C>T	NP_891555.2:p.Asn1334=
XM_011534477.1:c.4251C>T	XP_011532779.1:p.Asn1417=
XM_011534478.1:c.4233C>T	XP_011532780.1:p.Asn1411=
XM_011534482.1:c.4020C>T	XP_011532784.1:p.Asn1340=
XM_011534483.1:c.3942C>T	XP_011532785.1:p.Asn1314=
XM_011534484.1:c.3543C>T	XP_011532786.1:p.Asn1181=
XR_941095.1:n.4288C>T
XM_011534478.3:c.4233C>T	XP_011532780.1:p.Asn1411=
XM_011534484.2:c.3543C>T	XP_011532786.1:p.Asn1181=
XM_017009263.1:c.*148C>T	XP_016864752.1:n.*148C>T
XM_017009268.1:c.3924C>T	XP_016864757.1:p.Asn1308=
XR_001742050.2:n.4492C>T
NM_182925.5:c.4002C>T MANE Select	NP_891555.2:p.Asn1334=