Canonical Allele Identifier: CA405933781
Gene: LTBP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40605731C>A , CM000681.2:g.40605731C>A GRCh38
NC_000019.9:g.41111637C>A , CM000681.1:g.41111637C>A GRCh37
NC_000019.8:g.45803477C>A NCBI36
NG_021201.1:g.17566C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396819.8:c.693C>A MANE Select ENSP00000380031.5:p.Cys231Ter
ENST00000204005.13:c.783C>A ENSP00000204005.10:p.Cys261Ter
ENST00000308370.11:c.894C>A ENSP00000311905.8:p.Cys298Ter
ENST00000396819.7:c.693C>A ENSP00000380031.4:p.Cys231Ter
ENST00000598717.5:n.428+5628C>A
NM_001042544.1:c.894C>A NP_001036009.1:p.Cys298Ter
NM_001042545.1:c.693C>A NP_001036010.1:p.Cys231Ter
NM_003573.2:c.783C>A NP_003564.2:p.Cys261Ter
XM_011527376.1:c.894C>A XP_011525678.1:p.Cys298Ter
XM_011527377.1:c.927C>A XP_011525679.1:p.Cys309Ter
XM_011527378.1:c.927C>A XP_011525680.1:p.Cys309Ter
XM_011527379.1:c.693C>A XP_011525681.1:p.Cys231Ter
XM_011527380.1:c.927C>A XP_011525682.1:p.Cys309Ter
XM_011527381.1:c.927C>A XP_011525683.1:p.Cys309Ter
XM_011527382.1:c.927C>A XP_011525684.1:p.Cys309Ter
XM_011527383.1:c.927C>A XP_011525685.1:p.Cys309Ter
XM_011527384.1:c.927C>A XP_011525686.1:p.Cys309Ter
XM_011527385.1:c.927C>A XP_011525687.1:p.Cys309Ter
XM_011527386.1:c.927C>A XP_011525688.1:p.Cys309Ter
XM_011527387.1:c.285C>A XP_011525689.1:p.Cys95Ter
XM_011527376.2:c.894C>A XP_011525678.1:p.Cys298Ter
XM_011527377.2:c.927C>A XP_011525679.1:p.Cys309Ter
XM_011527378.2:c.927C>A XP_011525680.1:p.Cys309Ter
XM_011527380.2:c.927C>A XP_011525682.1:p.Cys309Ter
XM_011527381.2:c.927C>A XP_011525683.1:p.Cys309Ter
XM_011527382.2:c.927C>A XP_011525684.1:p.Cys309Ter
XM_011527383.2:c.927C>A XP_011525685.1:p.Cys309Ter
XM_011527384.2:c.927C>A XP_011525686.1:p.Cys309Ter
XM_011527385.2:c.927C>A XP_011525687.1:p.Cys309Ter
XM_011527386.2:c.927C>A XP_011525688.1:p.Cys309Ter
XM_017027352.1:c.927C>A XP_016882841.1:p.Cys309Ter
XM_017027353.1:c.927C>A XP_016882842.1:p.Cys309Ter
XM_017027354.1:c.927C>A XP_016882843.1:p.Cys309Ter
NM_001042545.2:c.693C>A MANE Select NP_001036010.1:p.Cys231Ter