Canonical Allele Identifier: CA1604713517

Gene: FLT4

Linked Data

• dbSNP Id: rs1761565314
• gnomAD v4: 5-180602493-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180602493T>C , CM000667.2:g.180602493T>C	GRCh38
NC_000005.9:g.180029493T>C , CM000667.1:g.180029493T>C	GRCh37
NC_000005.8:g.179962099T>C	NCBI36
NG_011536.1:g.52132A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261937.11:c.*699A>G MANE Select	ENSP00000261937.6:n.*699A>G
ENST00000261937.10:c.*699A>G	ENSP00000261937.6:n.*699A>G
NM_182925.4:c.*699A>G	NP_891555.2:n.*699A>G
XM_011534477.1:c.*699A>G	XP_011532779.1:n.*699A>G
XM_011534478.1:c.*699A>G	XP_011532780.1:n.*699A>G
XM_011534482.1:c.*699A>G	XP_011532784.1:n.*699A>G
XM_011534483.1:c.*699A>G	XP_011532785.1:n.*699A>G
XM_011534484.1:c.*699A>G	XP_011532786.1:n.*699A>G
XM_011534478.3:c.*699A>G	XP_011532780.1:n.*699A>G
XM_011534484.2:c.*699A>G	XP_011532786.1:n.*699A>G
XM_017009263.1:c.*937A>G	XP_016864752.1:n.*937A>G
XM_017009268.1:c.*699A>G	XP_016864757.1:n.*699A>G
XR_001742050.2:n.5281A>G
NM_182925.5:c.*699A>G MANE Select	NP_891555.2:n.*699A>G