Canonical Allele Identifier: CA10642832
Gene: LTBP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40600147C>G , CM000681.2:g.40600147C>G GRCh38
NC_000019.9:g.41106053C>G , CM000681.1:g.41106053C>G GRCh37
NC_000019.8:g.45797893C>G NCBI36
NG_021201.1:g.11982C>G

Transcript Alleles

HGVS Amino-acid Change
NM_001042544.1:c.421C>G NP_001036009.1:p.Pro141Ala
NM_003573.2:c.310C>G NP_003564.2:p.Pro104Ala
ENST00000204005.13:c.310C>G ENSP00000204005.10:p.Pro104Ala
ENST00000308370.11:c.421C>G ENSP00000311905.8:p.Pro141Ala
ENST00000593738.1:n.164C>G
ENST00000594537.2:c.*156C>G ENSP00000480629.1:n.*156C>G
ENST00000598717.5:n.428+44C>G
ENST00000599016.5:c.*156C>G ENSP00000482179.1:n.*156C>G
ENST00000600026.5:c.*156C>G ENSP00000483230.1:n.*156C>G
XM_011527376.1:c.421C>G XP_011525678.1:p.Pro141Ala
XM_011527376.2:c.421C>G XP_011525678.1:p.Pro141Ala
XM_011527377.1:c.454C>G XP_011525679.1:p.Pro152Ala
XM_011527377.2:c.454C>G XP_011525679.1:p.Pro152Ala
XM_011527378.1:c.454C>G XP_011525680.1:p.Pro152Ala
XM_011527378.2:c.454C>G XP_011525680.1:p.Pro152Ala
XM_011527380.1:c.454C>G XP_011525682.1:p.Pro152Ala
XM_011527380.2:c.454C>G XP_011525682.1:p.Pro152Ala
XM_011527381.1:c.454C>G XP_011525683.1:p.Pro152Ala
XM_011527381.2:c.454C>G XP_011525683.1:p.Pro152Ala
XM_011527382.1:c.454C>G XP_011525684.1:p.Pro152Ala
XM_011527382.2:c.454C>G XP_011525684.1:p.Pro152Ala
XM_011527383.1:c.454C>G XP_011525685.1:p.Pro152Ala
XM_011527383.2:c.454C>G XP_011525685.1:p.Pro152Ala
XM_011527384.1:c.454C>G XP_011525686.1:p.Pro152Ala
XM_011527384.2:c.454C>G XP_011525686.1:p.Pro152Ala
XM_011527385.1:c.454C>G XP_011525687.1:p.Pro152Ala
XM_011527385.2:c.454C>G XP_011525687.1:p.Pro152Ala
XM_011527386.1:c.454C>G XP_011525688.1:p.Pro152Ala
XM_011527386.2:c.454C>G XP_011525688.1:p.Pro152Ala
XM_011527387.1:c.-189C>G XP_011525689.1:n.-189C>G
XM_017027352.1:c.454C>G XP_016882841.1:p.Pro152Ala
XM_017027353.1:c.454C>G XP_016882842.1:p.Pro152Ala
XM_017027354.1:c.454C>G XP_016882843.1:p.Pro152Ala