Canonical Allele Identifier: CA362496386

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603388-C-G
• MyVariant Identifiers: chr5:g.180030388C>G (hg19) ; chr5:g.180603388C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603388C>G , CM000667.2:g.180603388C>G	GRCh38
NC_000005.9:g.180030388C>G , CM000667.1:g.180030388C>G	GRCh37
NC_000005.8:g.179962994C>G	NCBI36
NG_011536.1:g.51237G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3896G>C MANE Select	ENSP00000261937.6:p.Cys1299Ser
ENST00000261937.10:c.3896G>C	ENSP00000261937.6:p.Cys1299Ser
ENST00000502603.5:n.596G>C
NM_182925.4:c.3896G>C	NP_891555.2:p.Cys1299Ser
XM_011534477.1:c.4145G>C	XP_011532779.1:p.Cys1382Ser
XM_011534478.1:c.4127G>C	XP_011532780.1:p.Cys1376Ser
XM_011534479.1:c.*42G>C	XP_011532781.1:n.*42G>C
XM_011534482.1:c.3914G>C	XP_011532784.1:p.Cys1305Ser
XM_011534483.1:c.3836G>C	XP_011532785.1:p.Cys1279Ser
XM_011534484.1:c.3437G>C	XP_011532786.1:p.Cys1146Ser
XR_941095.1:n.4182G>C
XM_011534478.3:c.4127G>C	XP_011532780.1:p.Cys1376Ser
XM_011534484.2:c.3437G>C	XP_011532786.1:p.Cys1146Ser
XM_017009263.1:c.*42G>C	XP_016864752.1:n.*42G>C
XM_017009268.1:c.3818G>C	XP_016864757.1:p.Cys1273Ser
XR_001742050.2:n.4386G>C
NM_182925.5:c.3896G>C MANE Select	NP_891555.2:p.Cys1299Ser