Canonical Allele Identifier: CA362495352

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030202T>G (hg19) ; chr5:g.180603202T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603202T>G , CM000667.2:g.180603202T>G	GRCh38
NC_000005.9:g.180030202T>G , CM000667.1:g.180030202T>G	GRCh37
NC_000005.8:g.179962808T>G	NCBI36
NG_011536.1:g.51423A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4082A>C MANE Select	ENSP00000261937.6:p.Asn1361Thr
ENST00000261937.10:c.4082A>C	ENSP00000261937.6:p.Asn1361Thr
ENST00000502603.5:n.782A>C
NM_182925.4:c.4082A>C	NP_891555.2:p.Asn1361Thr
XM_011534477.1:c.4331A>C	XP_011532779.1:p.Asn1444Thr
XM_011534478.1:c.4313A>C	XP_011532780.1:p.Asn1438Thr
XM_011534482.1:c.4100A>C	XP_011532784.1:p.Asn1367Thr
XM_011534483.1:c.4022A>C	XP_011532785.1:p.Asn1341Thr
XM_011534484.1:c.3623A>C	XP_011532786.1:p.Asn1208Thr
XR_941095.1:n.4368A>C
XM_011534478.3:c.4313A>C	XP_011532780.1:p.Asn1438Thr
XM_011534484.2:c.3623A>C	XP_011532786.1:p.Asn1208Thr
XM_017009263.1:c.*228A>C	XP_016864752.1:n.*228A>C
XM_017009268.1:c.4004A>C	XP_016864757.1:p.Asn1335Thr
XR_001742050.2:n.4572A>C
NM_182925.5:c.4082A>C MANE Select	NP_891555.2:p.Asn1361Thr