Canonical Allele Identifier: CA1681247581

Gene: THBS2 THBS2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.169229658T= , CM000668.2:g.169229658T=	GRCh38
NC_000006.11:g.169629753T= , CM000668.1:g.169629753T=	GRCh37
NC_000006.10:g.169371678T=	NCBI36
NG_022911.1:g.29385A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617924.6:c.2173A= (THBS2) MANE Select	ENSP00000482784.1:p.Asn725=
ENST00000649844.1:c.2188A= (THBS2)	ENSP00000497834.1:p.Asn730=
ENST00000676498.1:c.2173A= (THBS2)	ENSP00000504820.1:p.Asn725=
ENST00000676628.1:c.1999A= (THBS2)	ENSP00000504416.1:p.Asn667=
ENST00000676760.1:c.2173A= (THBS2)	ENSP00000503020.1:p.Asn725=
ENST00000676869.1:c.2002A= (THBS2)	ENSP00000504488.1:p.Asn668=
ENST00000676941.1:c.1282A= (THBS2)	ENSP00000503028.1:p.Asn428=
ENST00000677429.1:c.*1539A= (THBS2)	ENSP00000503286.1:n.*1539A=
ENST00000678378.1:n.1558A= (THBS2)
ENST00000366787.7:c.2173A= (THBS2)	ENSP00000355751.3:p.Asn725=
ENST00000617924.4:c.2173A= (THBS2)	ENSP00000482784.1:p.Asn725=
NM_003247.3:c.2173A= (THBS2)	NP_003238.2:p.Asn725=
XR_943307.1:n.682-9567T= (THBS2-AS1)
NR_134621.1:n.682-9567T= (THBS2-AS1)
NM_003247.4:c.2173A= (THBS2)	NP_003238.2:p.Asn725=
NM_001381939.1:c.1999A= (THBS2)	NP_001368868.1:p.Asn667=
NM_001381942.1:c.1942A= (THBS2)	NP_001368871.1:p.Asn648=
NM_003247.5:c.2173A= (THBS2) MANE Select	NP_003238.2:p.Asn725=
NR_167744.1:n.2318A= (THBS2)
NR_167745.1:n.2447A= (THBS2)