Canonical Allele Identifier: CA2147075382

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74503472T= , CM000676.2:g.74503472T=	GRCh38
NC_000014.8:g.74970175T= , CM000676.1:g.74970175T=	GRCh37
NC_000014.7:g.74039928T=	NCBI36
NG_021486.1:g.113860A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261978.9:c.4717A= MANE Select	ENSP00000261978.4:p.Thr1573=
ENST00000261978.8:c.4717A=	ENSP00000261978.4:p.Thr1573=
ENST00000553939.5:c.4717A=	ENSP00000452110.1:p.Thr1573=
ENST00000556690.5:c.4585A=	ENSP00000451477.1:p.Thr1529=
NM_000428.2:c.4717A=	NP_000419.1:p.Thr1573=
XM_011536765.1:c.4336A=	XP_011535067.1:p.Thr1446=
XM_011536766.1:c.4258A=	XP_011535068.1:p.Thr1420=
XM_011536767.1:c.4234A=	XP_011535069.1:p.Thr1412=
XM_011536765.2:c.4336A=	XP_011535067.1:p.Thr1446=
NM_000428.3:c.4717A= MANE Select	NP_000419.1:p.Thr1573=