Canonical Allele Identifier: CA502131111

Gene: TIMP2 CEP295NL

Linked Data

• MyVariant Identifiers: chr17:g.76867008A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78870926A>G , CM000679.2:g.78870926A>G	GRCh38
NC_000017.10:g.76867008A>G , CM000679.1:g.76867008A>G	GRCh37
NC_000017.9:g.74378603A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586713.6:c.81T>C (TIMP2)	ENSP00000465968.2:p.Val27=
ENST00000706922.1:c.81T>C (TIMP2)	ENSP00000516642.1:p.Val27=
ENST00000706923.1:c.81T>C (TIMP2)	ENSP00000516643.1:p.Val27=
ENST00000262768.11:c.312T>C (TIMP2) MANE Select	ENSP00000262768.6:p.Val104=
ENST00000536189.6:c.81T>C (TIMP2)	ENSP00000441724.1:p.Val27=
ENST00000585421.5:c.81T>C (TIMP2)	ENSP00000467584.1:p.Val27=
ENST00000586057.5:c.81T>C (TIMP2)	ENSP00000468296.1:p.Val27=
ENST00000586713.5:c.81T>C (CEP295NL)	ENSP00000465968.1:p.Val27=
ENST00000592761.2:c.81T>C (TIMP2)	ENSP00000464930.1:p.Val27=
NM_003255.4:c.312T>C (TIMP2)	NP_003246.1:p.Val104=
NM_003255.5:c.312T>C (TIMP2) MANE Select	NP_003246.1:p.Val104=