Canonical Allele Identifier: CA2336068336
Gene: LTBP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40622551C= , CM000681.2:g.40622551C= GRCh38
NC_000019.9:g.41128456C= , CM000681.1:g.41128456C= GRCh37
NC_000019.8:g.45820296C= NCBI36
NG_021201.1:g.34386C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396819.8:c.3368C= MANE Select ENSP00000380031.5:p.Pro1123=
ENST00000204005.13:c.3458C= ENSP00000204005.10:p.Pro1153=
ENST00000243562.13:c.1567C=
ENST00000308370.11:c.3569C= ENSP00000311905.8:p.Pro1190=
ENST00000318809.11:n.484-1053C=
ENST00000396819.7:c.3368C= ENSP00000380031.4:p.Pro1123=
ENST00000593463.5:c.535-1053C=
ENST00000594116.1:n.164C=
ENST00000595118.5:n.873C=
ENST00000595665.1:n.535-1053C=
ENST00000597816.5:n.453-1053C=
ENST00000599724.5:c.485-1053C= ENSP00000469785.1:n.485-1053C=
ENST00000601032.5:c.1005C=
ENST00000622107.4:n.545-1053C=
ENST00000622457.1:c.385-1053C=
ENST00000622565.4:n.727-1053C=
NM_001042544.1:c.3569C= NP_001036009.1:p.Pro1190=
NM_001042545.1:c.3368C= NP_001036010.1:p.Pro1123=
NM_003573.2:c.3458C= NP_003564.2:p.Pro1153=
XM_011527376.1:c.3683C= XP_011525678.1:p.Pro1228=
XM_011527377.1:c.3602C= XP_011525679.1:p.Pro1201=
XM_011527378.1:c.3602C= XP_011525680.1:p.Pro1201=
XM_011527379.1:c.3482C= XP_011525681.1:p.Pro1161=
XM_011527380.1:c.3476C= XP_011525682.1:p.Pro1159=
XM_011527381.1:c.3476C= XP_011525683.1:p.Pro1159=
XM_011527382.1:c.3359C= XP_011525684.1:p.Pro1120=
XM_011527383.1:c.3452-1053C= XP_011525685.1:n.3452-1053C=
XM_011527384.1:c.3326-1053C= XP_011525686.1:n.3326-1053C=
XM_011527385.1:c.3320-1053C= XP_011525687.1:n.3320-1053C=
XM_011527386.1:c.3194-1053C= XP_011525688.1:n.3194-1053C=
XM_011527387.1:c.2960C= XP_011525689.1:p.Pro987=
XM_011527376.2:c.3683C= XP_011525678.1:p.Pro1228=
XM_011527377.2:c.3602C= XP_011525679.1:p.Pro1201=
XM_011527378.2:c.3602C= XP_011525680.1:p.Pro1201=
XM_011527380.2:c.3476C= XP_011525682.1:p.Pro1159=
XM_011527381.2:c.3476C= XP_011525683.1:p.Pro1159=
XM_011527382.2:c.3359C= XP_011525684.1:p.Pro1120=
XM_011527383.2:c.3452-1053C= XP_011525685.1:n.3452-1053C=
XM_011527384.2:c.3326-1053C= XP_011525686.1:n.3326-1053C=
XM_011527385.2:c.3320-1053C= XP_011525687.1:n.3320-1053C=
XM_011527386.2:c.3194-1053C= XP_011525688.1:n.3194-1053C=
XM_017027352.1:c.3470C= XP_016882841.1:p.Pro1157=
XM_017027353.1:c.3344C= XP_016882842.1:p.Pro1115=
XM_017027354.1:c.3200-1053C= XP_016882843.1:n.3200-1053C=
NM_001042545.2:c.3368C= MANE Select NP_001036010.1:p.Pro1123=