Canonical Allele Identifier: CA2277198181

Gene: TIMP2 CEP295NL

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78870960G= , CM000679.2:g.78870960G=	GRCh38
NC_000017.10:g.76867042G= , CM000679.1:g.76867042G=	GRCh37
NC_000017.9:g.74378637G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586713.6:c.47C= (TIMP2)	ENSP00000465968.2:p.Pro16=
ENST00000706922.1:c.47C= (TIMP2)	ENSP00000516642.1:p.Pro16=
ENST00000706923.1:c.47C= (TIMP2)	ENSP00000516643.1:p.Pro16=
ENST00000262768.11:c.278C= (TIMP2) MANE Select	ENSP00000262768.6:p.Pro93=
ENST00000536189.6:c.47C= (TIMP2)	ENSP00000441724.1:p.Pro16=
ENST00000585421.5:c.47C= (TIMP2)	ENSP00000467584.1:p.Pro16=
ENST00000586057.5:c.47C= (TIMP2)	ENSP00000468296.1:p.Pro16=
ENST00000586713.5:c.47C= (CEP295NL)	ENSP00000465968.1:p.Pro16=
ENST00000592761.2:c.47C= (TIMP2)	ENSP00000464930.1:p.Pro16=
NM_003255.4:c.278C= (TIMP2)	NP_003246.1:p.Pro93=
NM_003255.5:c.278C= (TIMP2) MANE Select	NP_003246.1:p.Pro93=