Canonical Allele Identifier: CA362495760

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030275A>G (hg19) ; chr5:g.180603275A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603275A>G , CM000667.2:g.180603275A>G	GRCh38
NC_000005.9:g.180030275A>G , CM000667.1:g.180030275A>G	GRCh37
NC_000005.8:g.179962881A>G	NCBI36
NG_011536.1:g.51350T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4009T>C MANE Select	ENSP00000261937.6:p.Tyr1337His
ENST00000261937.10:c.4009T>C	ENSP00000261937.6:p.Tyr1337His
ENST00000502603.5:n.709T>C
NM_182925.4:c.4009T>C	NP_891555.2:p.Tyr1337His
XM_011534477.1:c.4258T>C	XP_011532779.1:p.Tyr1420His
XM_011534478.1:c.4240T>C	XP_011532780.1:p.Tyr1414His
XM_011534482.1:c.4027T>C	XP_011532784.1:p.Tyr1343His
XM_011534483.1:c.3949T>C	XP_011532785.1:p.Tyr1317His
XM_011534484.1:c.3550T>C	XP_011532786.1:p.Tyr1184His
XR_941095.1:n.4295T>C
XM_011534478.3:c.4240T>C	XP_011532780.1:p.Tyr1414His
XM_011534484.2:c.3550T>C	XP_011532786.1:p.Tyr1184His
XM_017009263.1:c.*155T>C	XP_016864752.1:n.*155T>C
XM_017009268.1:c.3931T>C	XP_016864757.1:p.Tyr1311His
XR_001742050.2:n.4499T>C
NM_182925.5:c.4009T>C MANE Select	NP_891555.2:p.Tyr1337His