Canonical Allele Identifier: CA2711056288

Gene: FLT4

Linked Data

• dbSNP Id: rs2127781918

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603465_180603466del , CM000667.2:g.180603465_180603466del	GRCh38
NC_000005.9:g.180030465_180030466del , CM000667.1:g.180030465_180030466del	GRCh37
NC_000005.8:g.179963071_179963072del	NCBI36
NG_011536.1:g.51159_51160del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3894-76_3894-75del MANE Select	ENSP00000261937.6:n.3894-76_3894-75del
ENST00000261937.10:c.3894-76_3894-75del	ENSP00000261937.6:n.3894-76_3894-75del
ENST00000502603.5:n.594-76_594-75del
NM_182925.4:c.3894-76_3894-75del	NP_891555.2:n.3894-76_3894-75del
XM_011534477.1:c.4143-76_4143-75del	XP_011532779.1:n.4143-76_4143-75del
XM_011534478.1:c.4125-76_4125-75del	XP_011532780.1:n.4125-76_4125-75del
XM_011534479.1:c.*40-76_*40-75del	XP_011532781.1:n.*40-76_*40-75del
XM_011534482.1:c.3912-76_3912-75del	XP_011532784.1:n.3912-76_3912-75del
XM_011534483.1:c.3834-76_3834-75del	XP_011532785.1:n.3834-76_3834-75del
XM_011534484.1:c.3435-76_3435-75del	XP_011532786.1:n.3435-76_3435-75del
XR_941095.1:n.4180-76_4180-75del
XM_011534478.3:c.4125-76_4125-75del	XP_011532780.1:n.4125-76_4125-75del
XM_011534484.2:c.3435-76_3435-75del	XP_011532786.1:n.3435-76_3435-75del
XM_017009263.1:c.*40-76_*40-75del	XP_016864752.1:n.*40-76_*40-75del
XM_017009268.1:c.3816-76_3816-75del	XP_016864757.1:n.3816-76_3816-75del
XR_001742050.2:n.4384-76_4384-75del
NM_182925.5:c.3894-76_3894-75del MANE Select	NP_891555.2:n.3894-76_3894-75del