Canonical Allele Identifier: CA2147073458

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74500985C= , CM000676.2:g.74500985C=	GRCh38
NC_000014.8:g.74967688C= , CM000676.1:g.74967688C=	GRCh37
NC_000014.7:g.74037441C=	NCBI36
NG_021486.1:g.116347G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261978.9:c.5365G= MANE Select	ENSP00000261978.4:p.Val1789=
ENST00000261978.8:c.5365G=	ENSP00000261978.4:p.Val1789=
ENST00000553939.5:c.*144G=	ENSP00000452110.1:n.*144G=
ENST00000554861.1:n.583G=
ENST00000556690.5:c.5233G=	ENSP00000451477.1:p.Val1745=
NM_000428.2:c.5365G=	NP_000419.1:p.Val1789=
XM_011536765.1:c.4984G=	XP_011535067.1:p.Val1662=
XM_011536766.1:c.4906G=	XP_011535068.1:p.Val1636=
XM_011536767.1:c.4882G=	XP_011535069.1:p.Val1628=
XM_011536765.2:c.4984G=	XP_011535067.1:p.Val1662=
NM_000428.3:c.5365G= MANE Select	NP_000419.1:p.Val1789=