Canonical Allele Identifier: CA362496281

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030370T>G (hg19) ; chr5:g.180603370T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603370T>G , CM000667.2:g.180603370T>G	GRCh38
NC_000005.9:g.180030370T>G , CM000667.1:g.180030370T>G	GRCh37
NC_000005.8:g.179962976T>G	NCBI36
NG_011536.1:g.51255A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3914A>C MANE Select	ENSP00000261937.6:p.Asn1305Thr
ENST00000261937.10:c.3914A>C	ENSP00000261937.6:p.Asn1305Thr
ENST00000502603.5:n.614A>C
NM_182925.4:c.3914A>C	NP_891555.2:p.Asn1305Thr
XM_011534477.1:c.4163A>C	XP_011532779.1:p.Asn1388Thr
XM_011534478.1:c.4145A>C	XP_011532780.1:p.Asn1382Thr
XM_011534479.1:c.*60A>C	XP_011532781.1:n.*60A>C
XM_011534482.1:c.3932A>C	XP_011532784.1:p.Asn1311Thr
XM_011534483.1:c.3854A>C	XP_011532785.1:p.Asn1285Thr
XM_011534484.1:c.3455A>C	XP_011532786.1:p.Asn1152Thr
XR_941095.1:n.4200A>C
XM_011534478.3:c.4145A>C	XP_011532780.1:p.Asn1382Thr
XM_011534484.2:c.3455A>C	XP_011532786.1:p.Asn1152Thr
XM_017009263.1:c.*60A>C	XP_016864752.1:n.*60A>C
XM_017009268.1:c.3836A>C	XP_016864757.1:p.Asn1279Thr
XR_001742050.2:n.4404A>C
NM_182925.5:c.3914A>C MANE Select	NP_891555.2:p.Asn1305Thr