Canonical Allele Identifier: CA2676967844

Gene: FLT4

Linked Data

• gnomAD v4: 5-180603501-C-CTGAACCCCCAAGTGCTGGGGGTCTTGTCCGATGCTGCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180603501_180603502insTGAACCCCCAAGTGCTGGGGGTCTTGTCCGATGCTGCTT , CM000667.2:g.180603501_180603502insTGAACCCCCAAGTGCTGGGGGTCTTGTCCGATGCTGCTT	GRCh38
NC_000005.9:g.180030501_180030502insTGAACCCCCAAGTGCTGGGGGTCTTGTCCGATGCTGCTT , CM000667.1:g.180030501_180030502insTGAACCCCCAAGTGCTGGGGGTCTTGTCCGATGCTGCTT	GRCh37
NC_000005.8:g.179963107_179963108insTGAACCCCCAAGTGCTGGGGGTCTTGTCCGATGCTGCTT	NCBI36
NG_011536.1:g.51123_51124insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3894-112_3894-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA MANE Select	ENSP00000261937.6:n.3894-112_3894-111insAAGCAGCATCGGACAAGACCC...
ENST00000261937.10:c.3894-112_3894-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA	ENSP00000261937.6:n.3894-112_3894-111insAAGCAGCATCGGACAAGACCC...
ENST00000502603.5:n.594-112_594-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA
NM_182925.4:c.3894-112_3894-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA	NP_891555.2:n.3894-112_3894-111insAAGCAGCATCGGACAAGACCCCCAGCA...
XM_011534477.1:c.4143-112_4143-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA	XP_011532779.1:n.4143-112_4143-111insAAGCAGCATCGGACAAGACCCCCA...
XM_011534478.1:c.4125-112_4125-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA	XP_011532780.1:n.4125-112_4125-111insAAGCAGCATCGGACAAGACCCCCA...
XM_011534479.1:c.*40-112_*40-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA	XP_011532781.1:n.*40-112_*40-111insAAGCAGCATCGGACAAGACCCCCAGC...
XM_011534482.1:c.3912-112_3912-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA	XP_011532784.1:n.3912-112_3912-111insAAGCAGCATCGGACAAGACCCCCA...
XM_011534483.1:c.3834-112_3834-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA	XP_011532785.1:n.3834-112_3834-111insAAGCAGCATCGGACAAGACCCCCA...
XM_011534484.1:c.3435-112_3435-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA	XP_011532786.1:n.3435-112_3435-111insAAGCAGCATCGGACAAGACCCCCA...
XR_941095.1:n.4180-112_4180-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA
XM_011534478.3:c.4125-112_4125-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA	XP_011532780.1:n.4125-112_4125-111insAAGCAGCATCGGACAAGACCCCCA...
XM_011534484.2:c.3435-112_3435-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA	XP_011532786.1:n.3435-112_3435-111insAAGCAGCATCGGACAAGACCCCCA...
XM_017009263.1:c.*40-112_*40-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA	XP_016864752.1:n.*40-112_*40-111insAAGCAGCATCGGACAAGACCCCCAGC...
XM_017009268.1:c.3816-112_3816-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA	XP_016864757.1:n.3816-112_3816-111insAAGCAGCATCGGACAAGACCCCCA...
XR_001742050.2:n.4384-112_4384-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA
NM_182925.5:c.3894-112_3894-111insAAGCAGCATCGGACAAGACCCCCAGCACTTGGGGGTTCA MANE Select	NP_891555.2:n.3894-112_3894-111insAAGCAGCATCGGACAAGACCCCCAGCA...