Canonical Allele Identifier: CA448099110

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603363-A-G
• MyVariant Identifiers: chr5:g.180030363A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603363A>G , CM000667.2:g.180603363A>G	GRCh38
NC_000005.9:g.180030363A>G , CM000667.1:g.180030363A>G	GRCh37
NC_000005.8:g.179962969A>G	NCBI36
NG_011536.1:g.51262T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3921T>C MANE Select	ENSP00000261937.6:p.Ala1307=
ENST00000261937.10:c.3921T>C	ENSP00000261937.6:p.Ala1307=
ENST00000502603.5:n.621T>C
NM_182925.4:c.3921T>C	NP_891555.2:p.Ala1307=
XM_011534477.1:c.4170T>C	XP_011532779.1:p.Ala1390=
XM_011534478.1:c.4152T>C	XP_011532780.1:p.Ala1384=
XM_011534479.1:c.*67T>C	XP_011532781.1:n.*67T>C
XM_011534482.1:c.3939T>C	XP_011532784.1:p.Ala1313=
XM_011534483.1:c.3861T>C	XP_011532785.1:p.Ala1287=
XM_011534484.1:c.3462T>C	XP_011532786.1:p.Ala1154=
XR_941095.1:n.4207T>C
XM_011534478.3:c.4152T>C	XP_011532780.1:p.Ala1384=
XM_011534484.2:c.3462T>C	XP_011532786.1:p.Ala1154=
XM_017009263.1:c.*67T>C	XP_016864752.1:n.*67T>C
XM_017009268.1:c.3843T>C	XP_016864757.1:p.Ala1281=
XR_001742050.2:n.4411T>C
NM_182925.5:c.3921T>C MANE Select	NP_891555.2:p.Ala1307=