Canonical Allele Identifier: CA2336068363
Gene: LTBP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40622615T= , CM000681.2:g.40622615T= GRCh38
NC_000019.9:g.41128520T= , CM000681.1:g.41128520T= GRCh37
NC_000019.8:g.45820360T= NCBI36
NG_021201.1:g.34450T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396819.8:c.3432T= MANE Select ENSP00000380031.5:p.Gly1144=
ENST00000204005.13:c.3522T= ENSP00000204005.10:p.Gly1174=
ENST00000243562.13:c.1631T=
ENST00000308370.11:c.3633T= ENSP00000311905.8:p.Gly1211=
ENST00000318809.11:n.484-989T=
ENST00000396819.7:c.3432T= ENSP00000380031.4:p.Gly1144=
ENST00000593463.5:c.535-989T=
ENST00000594116.1:n.228T=
ENST00000595118.5:n.937T=
ENST00000595665.1:n.535-989T=
ENST00000597816.5:n.453-989T=
ENST00000599724.5:c.485-989T= ENSP00000469785.1:n.485-989T=
ENST00000601032.5:c.1069T=
ENST00000622107.4:n.545-989T=
ENST00000622457.1:c.385-989T=
ENST00000622565.4:n.727-989T=
NM_001042544.1:c.3633T= NP_001036009.1:p.Gly1211=
NM_001042545.1:c.3432T= NP_001036010.1:p.Gly1144=
NM_003573.2:c.3522T= NP_003564.2:p.Gly1174=
XM_011527376.1:c.3747T= XP_011525678.1:p.Gly1249=
XM_011527377.1:c.3666T= XP_011525679.1:p.Gly1222=
XM_011527378.1:c.3666T= XP_011525680.1:p.Gly1222=
XM_011527379.1:c.3546T= XP_011525681.1:p.Gly1182=
XM_011527380.1:c.3540T= XP_011525682.1:p.Gly1180=
XM_011527381.1:c.3540T= XP_011525683.1:p.Gly1180=
XM_011527382.1:c.3423T= XP_011525684.1:p.Gly1141=
XM_011527383.1:c.3452-989T= XP_011525685.1:n.3452-989T=
XM_011527384.1:c.3326-989T= XP_011525686.1:n.3326-989T=
XM_011527385.1:c.3320-989T= XP_011525687.1:n.3320-989T=
XM_011527386.1:c.3194-989T= XP_011525688.1:n.3194-989T=
XM_011527387.1:c.3024T= XP_011525689.1:p.Gly1008=
XM_011527376.2:c.3747T= XP_011525678.1:p.Gly1249=
XM_011527377.2:c.3666T= XP_011525679.1:p.Gly1222=
XM_011527378.2:c.3666T= XP_011525680.1:p.Gly1222=
XM_011527380.2:c.3540T= XP_011525682.1:p.Gly1180=
XM_011527381.2:c.3540T= XP_011525683.1:p.Gly1180=
XM_011527382.2:c.3423T= XP_011525684.1:p.Gly1141=
XM_011527383.2:c.3452-989T= XP_011525685.1:n.3452-989T=
XM_011527384.2:c.3326-989T= XP_011525686.1:n.3326-989T=
XM_011527385.2:c.3320-989T= XP_011525687.1:n.3320-989T=
XM_011527386.2:c.3194-989T= XP_011525688.1:n.3194-989T=
XM_017027352.1:c.3534T= XP_016882841.1:p.Gly1178=
XM_017027353.1:c.3408T= XP_016882842.1:p.Gly1136=
XM_017027354.1:c.3200-989T= XP_016882843.1:n.3200-989T=
NM_001042545.2:c.3432T= MANE Select NP_001036010.1:p.Gly1144=