Canonical Allele Identifier: CA2147096561

Gene: LTBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74552291G= , CM000676.2:g.74552291G=	GRCh38
NC_000014.8:g.75018994G= , CM000676.1:g.75018994G=	GRCh37
NC_000014.7:g.74088747G=	NCBI36
NG_021486.1:g.65041C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000428.3:c.1295C= MANE Select	NP_000419.1:p.Pro432=
ENST00000261978.9:c.1295C= MANE Select	ENSP00000261978.4:p.Pro432=
NM_000428.2:c.1295C=	NP_000419.1:p.Pro432=
ENST00000261978.8:c.1295C=	ENSP00000261978.4:p.Pro432=
ENST00000553939.5:c.1295C=	ENSP00000452110.1:p.Pro432=
ENST00000556690.5:c.1295C=	ENSP00000451477.1:p.Pro432=
ENST00000557425.1:n.124-941C=
XM_011536765.1:c.1295C=	XP_011535067.1:p.Pro432=
XM_011536765.2:c.1295C=	XP_011535067.1:p.Pro432=
XM_011536766.1:c.836C=	XP_011535068.1:p.Pro279=
XM_011536767.1:c.812C=	XP_011535069.1:p.Pro271=