Canonical Allele Identifier: CA1979272382

Gene: LTBP3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65539297C= , CM000673.2:g.65539297C=	GRCh38
NC_000011.9:g.65306768C= , CM000673.1:g.65306768C=	GRCh37
NC_000011.8:g.65063344C=	NCBI36
NG_016437.1:g.23932G=
NG_047172.1:g.19233C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001130144.3:c.3760+31G= MANE Select	NP_001123616.1:n.3760+31G=
ENST00000301873.11:c.3760+31G= MANE Select	ENSP00000301873.5:n.3760+31G=
NM_001130144.2:c.3760+31G=	NP_001123616.1:n.3760+31G=
NM_001164266.1:c.3268+31G=	NP_001157738.1:n.3268+31G=
NM_021070.4:c.3619+31G=	NP_066548.2:n.3619+31G=
ENST00000301873.9:c.3760+31G=	ENSP00000301873.5:n.3760+31G=
ENST00000322147.8:c.3619+31G=	ENSP00000326647.4:n.3619+31G=
ENST00000526825.6:c.*3023+31G=	ENSP00000435146.2:n.*3023+31G=
ENST00000526927.5:c.2570+31G=
ENST00000526927.6:c.2764+31G=	ENSP00000431219.2:n.2764+31G=
ENST00000528516.5:c.*3264+31G=	ENSP00000432350.1:n.*3264+31G=
ENST00000529189.5:c.628+31G=	ENSP00000434406.1:n.628+31G=
ENST00000529582.5:n.1474+31G=
ENST00000529582.6:n.1802+31G=
ENST00000530785.5:c.769+31G=	ENSP00000434315.1:n.769+31G=
ENST00000530866.6:c.3493+31G=	ENSP00000435276.2:n.3493+31G=
ENST00000532661.5:c.628+31G=	ENSP00000436341.1:n.628+31G=
ENST00000532661.6:c.628+31G=	ENSP00000436341.2:n.628+31G=
ENST00000532932.5:c.2050+31G=	ENSP00000435530.1:n.2050+31G=
ENST00000536982.5:c.768+31G=	ENSP00000441912.2:n.768+31G=
ENST00000685178.1:n.3291+31G=
ENST00000688764.1:n.2120+31G=
ENST00000689505.1:c.3637+31G=	ENSP00000510401.1:n.3637+31G=
XM_011545032.1:c.3787+31G=	XP_011543334.1:n.3787+31G=
XM_011545032.2:c.3787+31G=	XP_011543334.1:n.3787+31G=
XM_011545033.1:c.3646+31G=	XP_011543335.1:n.3646+31G=
XM_011545033.3:c.3646+31G=	XP_011543335.1:n.3646+31G=
XR_001747875.2:n.4227+31G=
XR_949928.3:n.4086+31G=