Canonical Allele Identifier: CA2147073461

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74500988A= , CM000676.2:g.74500988A=	GRCh38
NC_000014.8:g.74967691A= , CM000676.1:g.74967691A=	GRCh37
NC_000014.7:g.74037444A=	NCBI36
NG_021486.1:g.116344T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261978.9:c.5362T= MANE Select	ENSP00000261978.4:p.Cys1788=
ENST00000261978.8:c.5362T=	ENSP00000261978.4:p.Cys1788=
ENST00000553939.5:c.*141T=	ENSP00000452110.1:n.*141T=
ENST00000554861.1:n.580T=
ENST00000556690.5:c.5230T=	ENSP00000451477.1:p.Cys1744=
NM_000428.2:c.5362T=	NP_000419.1:p.Cys1788=
XM_011536765.1:c.4981T=	XP_011535067.1:p.Cys1661=
XM_011536766.1:c.4903T=	XP_011535068.1:p.Cys1635=
XM_011536767.1:c.4879T=	XP_011535069.1:p.Cys1627=
XM_011536765.2:c.4981T=	XP_011535067.1:p.Cys1661=
NM_000428.3:c.5362T= MANE Select	NP_000419.1:p.Cys1788=