Canonical Allele Identifier: CA2625678409

Gene: LTBP2

Linked Data

• gnomAD v4: 14-74611622-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74611625del , CM000676.2:g.74611625del	GRCh38
NC_000014.8:g.75078328del , CM000676.1:g.75078328del	GRCh37
NC_000014.7:g.74148081del	NCBI36
NG_021486.1:g.5709del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.322del MANE Select	ENSP00000261978.4:p.Arg108AlafsTer?
ENST00000261978.8:c.322del	ENSP00000261978.4:p.Arg108AlafsTer?
ENST00000553939.5:c.322del	ENSP00000452110.1:p.Arg108AlafsTer?
ENST00000556690.5:c.322del	ENSP00000451477.1:p.Arg108AlafsTer?
ENST00000557425.1:n.123+423del
NM_000428.2:c.322del	NP_000419.1:p.Arg108AlafsTer?
XM_011536765.1:c.322del	XP_011535067.1:p.Arg108AlafsTer?
XM_011536767.1:c.11+6961del	XP_011535069.1:n.11+6961del
XM_011536765.2:c.322del	XP_011535067.1:p.Arg108AlafsTer?
NM_000428.3:c.322del MANE Select	NP_000419.1:p.Arg108AlafsTer?