Canonical Allele Identifier: CA2802156168

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74501081_74501082insA , CM000676.2:g.74501081_74501082insA	GRCh38
NC_000014.8:g.74967784_74967785insA , CM000676.1:g.74967784_74967785insA	GRCh37
NC_000014.7:g.74037537_74037538insA	NCBI36
NG_021486.1:g.116250_116251insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.5321-53_5321-52insT MANE Select	ENSP00000261978.4:n.5321-53_5321-52insT
ENST00000261978.8:c.5321-53_5321-52insT	ENSP00000261978.4:n.5321-53_5321-52insT
ENST00000553939.5:c.*100-53_*100-52insT	ENSP00000452110.1:n.*100-53_*100-52insT
ENST00000554861.1:n.539-53_539-52insT
ENST00000556690.5:c.5189-53_5189-52insT	ENSP00000451477.1:n.5189-53_5189-52insT
NM_000428.2:c.5321-53_5321-52insT	NP_000419.1:n.5321-53_5321-52insT
XM_011536765.1:c.4940-53_4940-52insT	XP_011535067.1:n.4940-53_4940-52insT
XM_011536766.1:c.4862-53_4862-52insT	XP_011535068.1:n.4862-53_4862-52insT
XM_011536767.1:c.4838-53_4838-52insT	XP_011535069.1:n.4838-53_4838-52insT
XM_011536765.2:c.4940-53_4940-52insT	XP_011535067.1:n.4940-53_4940-52insT
NM_000428.3:c.5321-53_5321-52insT MANE Select	NP_000419.1:n.5321-53_5321-52insT