Canonical Allele Identifier: CA448098951

Gene: FLT4

Linked Data

• MyVariant Identifiers: chr5:g.180030216A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603216A>G , CM000667.2:g.180603216A>G	GRCh38
NC_000005.9:g.180030216A>G , CM000667.1:g.180030216A>G	GRCh37
NC_000005.8:g.179962822A>G	NCBI36
NG_011536.1:g.51409T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.4068T>C MANE Select	ENSP00000261937.6:p.Thr1356=
ENST00000261937.10:c.4068T>C	ENSP00000261937.6:p.Thr1356=
ENST00000502603.5:n.768T>C
NM_182925.4:c.4068T>C	NP_891555.2:p.Thr1356=
XM_011534477.1:c.4317T>C	XP_011532779.1:p.Thr1439=
XM_011534478.1:c.4299T>C	XP_011532780.1:p.Thr1433=
XM_011534482.1:c.4086T>C	XP_011532784.1:p.Thr1362=
XM_011534483.1:c.4008T>C	XP_011532785.1:p.Thr1336=
XM_011534484.1:c.3609T>C	XP_011532786.1:p.Thr1203=
XR_941095.1:n.4354T>C
XM_011534478.3:c.4299T>C	XP_011532780.1:p.Thr1433=
XM_011534484.2:c.3609T>C	XP_011532786.1:p.Thr1203=
XM_017009263.1:c.*214T>C	XP_016864752.1:n.*214T>C
XM_017009268.1:c.3990T>C	XP_016864757.1:p.Thr1330=
XR_001742050.2:n.4558T>C
NM_182925.5:c.4068T>C MANE Select	NP_891555.2:p.Thr1356=