Canonical Allele Identifier: CA2695228752

Gene: LTBP4

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40613452_40613453delinsAA , CM000681.2:g.40613452_40613453delinsAA	GRCh38
NC_000019.9:g.41119358_41119359delinsAA , CM000681.1:g.41119358_41119359delinsAA	GRCh37
NC_000019.8:g.45811198_45811199delinsAA	NCBI36
NG_021201.1:g.25287_25288delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396819.8:c.2480_2481delinsAA MANE Select	ENSP00000380031.5:p.Cys827Ter
ENST00000204005.13:c.2570_2571delinsAA	ENSP00000204005.10:p.Cys857Ter
ENST00000243562.13:c.679_680delinsAA
ENST00000308370.11:c.2681_2682delinsAA	ENSP00000311905.8:p.Cys894Ter
ENST00000396819.7:c.2480_2481delinsAA	ENSP00000380031.4:p.Cys827Ter
ENST00000546155.5:n.909_910delinsAA
ENST00000599724.5:c.5_6delinsAA	ENSP00000469785.1:p.Cys2Ter
ENST00000600499.5:n.80_81delinsAA
ENST00000601032.5:c.375_376delinsAA
ENST00000610893.4:n.78_79delinsAA
ENST00000612121.4:c.111_112delinsAA
ENST00000612845.4:n.39_40delinsAA
NM_001042544.1:c.2681_2682delinsAA	NP_001036009.1:p.Cys894Ter
NM_001042545.1:c.2480_2481delinsAA	NP_001036010.1:p.Cys827Ter
NM_003573.2:c.2570_2571delinsAA	NP_003564.2:p.Cys857Ter
XM_011527376.1:c.2795_2796delinsAA	XP_011525678.1:p.Cys932Ter
XM_011527377.1:c.2714_2715delinsAA	XP_011525679.1:p.Cys905Ter
XM_011527378.1:c.2714_2715delinsAA	XP_011525680.1:p.Cys905Ter
XM_011527379.1:c.2594_2595delinsAA	XP_011525681.1:p.Cys865Ter
XM_011527380.1:c.2588_2589delinsAA	XP_011525682.1:p.Cys863Ter
XM_011527381.1:c.2714_2715delinsAA	XP_011525683.1:p.Cys905Ter
XM_011527382.1:c.2471_2472delinsAA	XP_011525684.1:p.Cys824Ter
XM_011527383.1:c.2714_2715delinsAA	XP_011525685.1:p.Cys905Ter
XM_011527384.1:c.2714_2715delinsAA	XP_011525686.1:p.Cys905Ter
XM_011527385.1:c.2714_2715delinsAA	XP_011525687.1:p.Cys905Ter
XM_011527386.1:c.2714_2715delinsAA	XP_011525688.1:p.Cys905Ter
XM_011527387.1:c.2072_2073delinsAA	XP_011525689.1:p.Cys691Ter
XM_011527376.2:c.2795_2796delinsAA	XP_011525678.1:p.Cys932Ter
XM_011527377.2:c.2714_2715delinsAA	XP_011525679.1:p.Cys905Ter
XM_011527378.2:c.2714_2715delinsAA	XP_011525680.1:p.Cys905Ter
XM_011527380.2:c.2588_2589delinsAA	XP_011525682.1:p.Cys863Ter
XM_011527381.2:c.2714_2715delinsAA	XP_011525683.1:p.Cys905Ter
XM_011527382.2:c.2471_2472delinsAA	XP_011525684.1:p.Cys824Ter
XM_011527383.2:c.2714_2715delinsAA	XP_011525685.1:p.Cys905Ter
XM_011527384.2:c.2714_2715delinsAA	XP_011525686.1:p.Cys905Ter
XM_011527385.2:c.2714_2715delinsAA	XP_011525687.1:p.Cys905Ter
XM_011527386.2:c.2714_2715delinsAA	XP_011525688.1:p.Cys905Ter
XM_017027352.1:c.2714_2715delinsAA	XP_016882841.1:p.Cys905Ter
XM_017027353.1:c.2714_2715delinsAA	XP_016882842.1:p.Cys905Ter
XM_017027354.1:c.2588_2589delinsAA	XP_016882843.1:p.Cys863Ter
NM_001042545.2:c.2480_2481delinsAA MANE Select	NP_001036010.1:p.Cys827Ter