Canonical Allele Identifier: CA919452135

Gene: LTBP2

Linked Data

• dbSNP Id: rs1566610489

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74501043_74501044del , CM000676.2:g.74501043_74501044del	GRCh38
NC_000014.8:g.74967746_74967747del , CM000676.1:g.74967746_74967747del	GRCh37
NC_000014.7:g.74037499_74037500del	NCBI36
NG_021486.1:g.116289_116290del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.5321-14_5321-13del MANE Select	ENSP00000261978.4:n.5321-14_5321-13del
ENST00000261978.8:c.5321-14_5321-13del	ENSP00000261978.4:n.5321-14_5321-13del
ENST00000553939.5:c.*100-14_*100-13del	ENSP00000452110.1:n.*100-14_*100-13del
ENST00000554861.1:n.539-14_539-13del
ENST00000556690.5:c.5189-14_5189-13del	ENSP00000451477.1:n.5189-14_5189-13del
NM_000428.2:c.5321-14_5321-13del	NP_000419.1:n.5321-14_5321-13del
XM_011536765.1:c.4940-14_4940-13del	XP_011535067.1:n.4940-14_4940-13del
XM_011536766.1:c.4862-14_4862-13del	XP_011535068.1:n.4862-14_4862-13del
XM_011536767.1:c.4838-14_4838-13del	XP_011535069.1:n.4838-14_4838-13del
XM_011536765.2:c.4940-14_4940-13del	XP_011535067.1:n.4940-14_4940-13del
NM_000428.3:c.5321-14_5321-13del MANE Select	NP_000419.1:n.5321-14_5321-13del