Canonical Allele Identifier: CA362496279

Gene: FLT4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3914A>G MANE Select	ENSP00000261937.6:p.Asn1305Ser
ENST00000261937.10:c.3914A>G	ENSP00000261937.6:p.Asn1305Ser
ENST00000502603.5:n.614A>G
NM_182925.4:c.3914A>G	NP_891555.2:p.Asn1305Ser
XM_011534477.1:c.4163A>G	XP_011532779.1:p.Asn1388Ser
XM_011534478.1:c.4145A>G	XP_011532780.1:p.Asn1382Ser
XM_011534479.1:c.*60A>G	XP_011532781.1:n.*60A>G
XM_011534482.1:c.3932A>G	XP_011532784.1:p.Asn1311Ser
XM_011534483.1:c.3854A>G	XP_011532785.1:p.Asn1285Ser
XM_011534484.1:c.3455A>G	XP_011532786.1:p.Asn1152Ser
XR_941095.1:n.4200A>G
XM_011534478.3:c.4145A>G	XP_011532780.1:p.Asn1382Ser
XM_011534484.2:c.3455A>G	XP_011532786.1:p.Asn1152Ser
XM_017009263.1:c.*60A>G	XP_016864752.1:n.*60A>G
XM_017009268.1:c.3836A>G	XP_016864757.1:p.Asn1279Ser
XR_001742050.2:n.4404A>G
NM_182925.5:c.3914A>G MANE Select	NP_891555.2:p.Asn1305Ser