Canonical Allele Identifier: CA2802162429

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74611620_74611621insAGA , CM000676.2:g.74611620_74611621insAGA	GRCh38
NC_000014.8:g.75078323_75078324insAGA , CM000676.1:g.75078323_75078324insAGA	GRCh37
NC_000014.7:g.74148076_74148077insAGA	NCBI36
NG_021486.1:g.5711_5712insTCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000261978.9:c.324_325insTCT MANE Select	ENSP00000261978.4:p.Arg108_Ala109insSer
ENST00000261978.8:c.324_325insTCT	ENSP00000261978.4:p.Arg108_Ala109insSer
ENST00000553939.5:c.324_325insTCT	ENSP00000452110.1:p.Arg108_Ala109insSer
ENST00000556690.5:c.324_325insTCT	ENSP00000451477.1:p.Arg108_Ala109insSer
ENST00000557425.1:n.123+425_123+426insTCT
NM_000428.2:c.324_325insTCT	NP_000419.1:p.Arg108_Ala109insSer
XM_011536765.1:c.324_325insTCT	XP_011535067.1:p.Arg108_Ala109insSer
XM_011536767.1:c.11+6963_11+6964insTCT	XP_011535069.1:n.11+6963_11+6964insTCT
XM_011536765.2:c.324_325insTCT	XP_011535067.1:p.Arg108_Ala109insSer
NM_000428.3:c.324_325insTCT MANE Select	NP_000419.1:p.Arg108_Ala109insSer