Canonical Allele Identifier: CA2838210471

Gene: LTBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.33362463C>T , CM000664.2:g.33362463C>T	GRCh38
NC_000002.11:g.33587530C>T , CM000664.1:g.33587530C>T	GRCh37
NC_000002.10:g.33441034C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404816.7:c.4271-927C>T MANE Select	ENSP00000386043.2:n.4271-927C>T
ENST00000402934.5:c.3128-927C>T	ENSP00000384373.1:n.3128-927C>T
ENST00000404525.5:c.3134-927C>T	ENSP00000385359.1:n.3134-927C>T
ENST00000404816.6:c.4271-927C>T	ENSP00000386043.2:n.4271-927C>T
ENST00000407925.5:c.3293-927C>T	ENSP00000384091.1:n.3293-927C>T
ENST00000418533.6:c.3167-927C>T	ENSP00000393057.2:n.3167-927C>T
ENST00000422669.1:c.779-927C>T	ENSP00000395211.1:n.779-927C>T
NM_000627.3:c.3293-927C>T	NP_000618.3:n.3293-927C>T
NM_001166264.1:c.3167-927C>T	NP_001159736.1:n.3167-927C>T
NM_001166265.1:c.3134-927C>T	NP_001159737.1:n.3134-927C>T
NM_001166266.1:c.3008-927C>T	NP_001159738.1:n.3008-927C>T
NM_206943.2:c.4271-927C>T	NP_996826.2:n.4271-927C>T
XM_005264317.2:c.4112-927C>T	XP_005264374.1:n.4112-927C>T
XM_005264318.2:c.3986-927C>T	XP_005264375.1:n.3986-927C>T
XM_011532853.1:c.4274-927C>T	XP_011531155.1:n.4274-927C>T
XM_011532854.1:c.4271-927C>T	XP_011531156.1:n.4271-927C>T
XM_011532855.1:c.4268-927C>T	XP_011531157.1:n.4268-927C>T
XM_011532856.1:c.4154-927C>T	XP_011531158.1:n.4154-927C>T
XM_011532857.1:c.4148-927C>T	XP_011531159.1:n.4148-927C>T
XM_011532858.1:c.4148-927C>T	XP_011531160.1:n.4148-927C>T
XM_011532859.1:c.4115-927C>T	XP_011531161.1:n.4115-927C>T
XM_011532860.1:c.4106-927C>T	XP_011531162.1:n.4106-927C>T
XM_011532861.1:c.4004-927C>T	XP_011531163.1:n.4004-927C>T
XM_005264317.3:c.4112-927C>T	XP_005264374.1:n.4112-927C>T
XM_005264318.3:c.3986-927C>T	XP_005264375.1:n.3986-927C>T
XM_011532853.2:c.4274-927C>T	XP_011531155.1:n.4274-927C>T
XM_011532855.2:c.4268-927C>T	XP_011531157.1:n.4268-927C>T
XM_011532856.2:c.4154-927C>T	XP_011531158.1:n.4154-927C>T
XM_011532857.2:c.4148-927C>T	XP_011531159.1:n.4148-927C>T
XM_011532858.2:c.4148-927C>T	XP_011531160.1:n.4148-927C>T
XM_011532859.2:c.4115-927C>T	XP_011531161.1:n.4115-927C>T
XM_011532860.2:c.4106-927C>T	XP_011531162.1:n.4106-927C>T
XM_011532861.2:c.4004-927C>T	XP_011531163.1:n.4004-927C>T
XM_017004108.1:c.4151-927C>T	XP_016859597.1:n.4151-927C>T
XM_017004109.1:c.4145-927C>T	XP_016859598.1:n.4145-927C>T
XM_017004110.1:c.4025-927C>T	XP_016859599.1:n.4025-927C>T
XM_024452888.1:c.3677-927C>T	XP_024308656.1:n.3677-927C>T
XM_024452889.1:c.3677-927C>T	XP_024308657.1:n.3677-927C>T
XM_024452890.1:c.3041-927C>T	XP_024308658.1:n.3041-927C>T
NM_206943.3:c.4271-927C>T	NP_996826.2:n.4271-927C>T
NM_000627.4:c.3293-927C>T	NP_000618.4:n.3293-927C>T
NM_001166264.2:c.3167-927C>T	NP_001159736.2:n.3167-927C>T
NM_001166265.2:c.3134-927C>T	NP_001159737.2:n.3134-927C>T
NM_001166266.2:c.3008-927C>T	NP_001159738.2:n.3008-927C>T
NM_206943.4:c.4271-927C>T MANE Select	NP_996826.3:n.4271-927C>T
NM_001394905.1:c.4112-927C>T	NP_001381834.1:n.4112-927C>T
NM_001394906.1:c.3290-927C>T	NP_001381835.1:n.3290-927C>T
NM_001394907.1:c.3206-927C>T	NP_001381836.1:n.3206-927C>T
NM_001394908.1:c.3173-927C>T	NP_001381837.1:n.3173-927C>T
NM_001394909.1:c.3167-927C>T	NP_001381838.1:n.3167-927C>T
NM_001394910.1:c.3164-927C>T	NP_001381839.1:n.3164-927C>T
NM_001394911.1:c.3164-927C>T	NP_001381840.1:n.3164-927C>T
NM_001394912.1:c.3149-927C>T	NP_001381841.1:n.3149-927C>T
NM_001394913.1:c.3131-927C>T	NP_001381842.1:n.3131-927C>T
NM_001394914.1:c.3083-927C>T	NP_001381843.1:n.3083-927C>T
NM_001394915.1:c.3083-927C>T	NP_001381844.1:n.3083-927C>T
NM_001394916.1:c.3050-927C>T	NP_001381845.1:n.3050-927C>T
NM_001394917.1:c.3041-927C>T	NP_001381846.1:n.3041-927C>T
NM_001394918.1:c.3023-927C>T	NP_001381847.1:n.3023-927C>T
NM_001394919.1:c.3020-927C>T	NP_001381848.1:n.3020-927C>T
NM_001394920.1:c.3008-927C>T	NP_001381849.1:n.3008-927C>T
NM_001394921.1:c.3005-927C>T	NP_001381850.1:n.3005-927C>T
NM_001394923.1:c.2888-927C>T	NP_001381852.1:n.2888-927C>T
NM_001394924.1:c.2882-927C>T	NP_001381853.1:n.2882-927C>T
NM_001394925.1:c.2864-927C>T	NP_001381854.1:n.2864-927C>T
NM_001394926.1:c.2864-927C>T	NP_001381855.1:n.2864-927C>T
NM_001394927.1:c.2738-927C>T	NP_001381856.1:n.2738-927C>T