Canonical Allele Identifier: CA2711056292

Gene: FLT4

Linked Data

• dbSNP Id: rs2127781920

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603467_180603468insGCT , CM000667.2:g.180603467_180603468insGCT	GRCh38
NC_000005.9:g.180030467_180030468insGCT , CM000667.1:g.180030467_180030468insGCT	GRCh37
NC_000005.8:g.179963073_179963074insGCT	NCBI36
NG_011536.1:g.51157_51158insAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3894-78_3894-77insAGC MANE Select	ENSP00000261937.6:n.3894-78_3894-77insAGC
ENST00000261937.10:c.3894-78_3894-77insAGC	ENSP00000261937.6:n.3894-78_3894-77insAGC
ENST00000502603.5:n.594-78_594-77insAGC
NM_182925.4:c.3894-78_3894-77insAGC	NP_891555.2:n.3894-78_3894-77insAGC
XM_011534477.1:c.4143-78_4143-77insAGC	XP_011532779.1:n.4143-78_4143-77insAGC
XM_011534478.1:c.4125-78_4125-77insAGC	XP_011532780.1:n.4125-78_4125-77insAGC
XM_011534479.1:c.*40-78_*40-77insAGC	XP_011532781.1:n.*40-78_*40-77insAGC
XM_011534482.1:c.3912-78_3912-77insAGC	XP_011532784.1:n.3912-78_3912-77insAGC
XM_011534483.1:c.3834-78_3834-77insAGC	XP_011532785.1:n.3834-78_3834-77insAGC
XM_011534484.1:c.3435-78_3435-77insAGC	XP_011532786.1:n.3435-78_3435-77insAGC
XR_941095.1:n.4180-78_4180-77insAGC
XM_011534478.3:c.4125-78_4125-77insAGC	XP_011532780.1:n.4125-78_4125-77insAGC
XM_011534484.2:c.3435-78_3435-77insAGC	XP_011532786.1:n.3435-78_3435-77insAGC
XM_017009263.1:c.*40-78_*40-77insAGC	XP_016864752.1:n.*40-78_*40-77insAGC
XM_017009268.1:c.3816-78_3816-77insAGC	XP_016864757.1:n.3816-78_3816-77insAGC
XR_001742050.2:n.4384-78_4384-77insAGC
NM_182925.5:c.3894-78_3894-77insAGC MANE Select	NP_891555.2:n.3894-78_3894-77insAGC