Canonical Allele Identifier: CA2580614813

Gene: FLT4

Linked Data

• ClinVar Variation Id: 812613
• ClinVar RCV Id: RCV001003428

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180604767_180613470del , CM000667.2:g.180604767_180613470del	GRCh38
NC_000005.9:g.180031767_180040470del , CM000667.1:g.180031767_180040470del	GRCh37
NC_000005.8:g.179964373_179973076del	NCBI36
NG_011536.1:g.41159_49862del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3332-356_3894-1373del
ENST00000261937.10:c.3332-356_3894-1373del
NM_182925.4:c.3332-356_3894-1373del
XM_011534477.1:c.3581-356_4143-1373del
XM_011534478.1:c.3563-356_4125-1373del
XM_011534479.1:c.3581-356_*40-1373del
XM_011534482.1:c.3350-356_3912-1373del
XM_011534483.1:c.3272-356_3834-1373del
XM_011534484.1:c.2873-356_3435-1373del
XR_941095.1:n.3593-356_4180-1373del
XM_011534478.3:c.3563-356_4125-1373del
XM_011534484.2:c.2873-356_3435-1373del
XM_017009263.1:c.3563-356_*40-1373del
XM_017009268.1:c.3254-356_3816-1373del
XR_001742050.2:n.3797-356_4384-1373del
NM_182925.5:c.3332-356_3894-1373del