Canonical Allele Identifier: CA2676968872

Gene: FLT4

Linked Data

• gnomAD v4: 5-180609920-G-GTACCACAGA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.180609920_180609921insTACCACAGA , CM000667.2:g.180609920_180609921insTACCACAGA	GRCh38
NC_000005.9:g.180036920_180036921insTACCACAGA , CM000667.1:g.180036920_180036921insTACCACAGA	GRCh37
NC_000005.8:g.179969526_179969527insTACCACAGA	NCBI36
NG_011536.1:g.44704_44705insTCTGTGGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261937.11:c.3791_3792insTCTGTGGTA MANE Select	ENSP00000261937.6:p.Thr1264_Tyr1265insLeuTrpTyr
ENST00000261937.10:c.3791_3792insTCTGTGGTA	ENSP00000261937.6:p.Thr1264_Tyr1265insLeuTrpTyr
ENST00000393347.7:c.3791_3792insTCTGTGGTA	ENSP00000377016.3:p.Thr1264_Tyr1265insLeuTrpTyr
ENST00000502603.5:n.491_492insTCTGTGGTA
ENST00000502649.5:c.3791_3792insTCTGTGGTA	ENSP00000426057.1:p.Thr1264_Tyr1265insLeuTrpTyr
ENST00000507059.5:n.4141_4142insTCTGTGGTA
ENST00000619105.4:c.*2734_*2735insTCTGTGGTA	ENSP00000481134.1:n.*2734_*2735insTCTGTGGTA
NM_002020.4:c.3791_3792insTCTGTGGTA	NP_002011.2:p.Thr1264_Tyr1265insLeuTrpTyr
NM_182925.4:c.3791_3792insTCTGTGGTA	NP_891555.2:p.Thr1264_Tyr1265insLeuTrpTyr
XM_011534477.1:c.4040_4041insTCTGTGGTA	XP_011532779.1:p.Thr1347_Tyr1348insLeuTrpTyr
XM_011534478.1:c.4022_4023insTCTGTGGTA	XP_011532780.1:p.Thr1341_Tyr1342insLeuTrpTyr
XM_011534479.1:c.4040_4041insTCTGTGGTA	XP_011532781.1:p.Thr1347_Tyr1348insLeuTrpTyr
XM_011534480.1:c.4040_4041insTCTGTGGTA	XP_011532782.1:p.Thr1347_Tyr1348insLeuTrpTyr
XM_011534481.1:c.4040_4041insTCTGTGGTA	XP_011532783.1:p.Thr1347_Tyr1348insLeuTrpTyr
XM_011534482.1:c.3809_3810insTCTGTGGTA	XP_011532784.1:p.Thr1270_Tyr1271insLeuTrpTyr
XM_011534483.1:c.3731_3732insTCTGTGGTA	XP_011532785.1:p.Thr1244_Tyr1245insLeuTrpTyr
XM_011534484.1:c.3332_3333insTCTGTGGTA	XP_011532786.1:p.Thr1111_Tyr1112insLeuTrpTyr
XR_941095.1:n.4077_4078insTCTGTGGTA
NM_001354989.1:c.3791_3792insTCTGTGGTA	NP_001341918.1:p.Thr1264_Tyr1265insLeuTrpTyr
XM_011534478.3:c.4022_4023insTCTGTGGTA	XP_011532780.1:p.Thr1341_Tyr1342insLeuTrpTyr
XM_011534484.2:c.3332_3333insTCTGTGGTA	XP_011532786.1:p.Thr1111_Tyr1112insLeuTrpTyr
XM_017009263.1:c.4022_4023insTCTGTGGTA	XP_016864752.1:p.Thr1341_Tyr1342insLeuTrpTyr
XM_017009264.2:c.4022_4023insTCTGTGGTA	XP_016864753.1:p.Thr1341_Tyr1342insLeuTrpTyr
XM_017009265.1:c.4022_4023insTCTGTGGTA	XP_016864754.1:p.Thr1341_Tyr1342insLeuTrpTyr
XM_017009266.1:c.4022_4023insTCTGTGGTA	XP_016864755.1:p.Thr1341_Tyr1342insLeuTrpTyr
XM_017009267.2:c.4022_4023insTCTGTGGTA	XP_016864756.1:p.Thr1341_Tyr1342insLeuTrpTyr
XM_017009268.1:c.3713_3714insTCTGTGGTA	XP_016864757.1:p.Thr1238_Tyr1239insLeuTrpTyr
XR_001742050.2:n.4281_4282insTCTGTGGTA
NM_182925.5:c.3791_3792insTCTGTGGTA MANE Select	NP_891555.2:p.Thr1264_Tyr1265insLeuTrpTyr
NM_001354989.2:c.3791_3792insTCTGTGGTA	NP_001341918.1:p.Thr1264_Tyr1265insLeuTrpTyr
NM_002020.5:c.3791_3792insTCTGTGGTA	NP_002011.2:p.Thr1264_Tyr1265insLeuTrpTyr