Canonical Allele Identifier: CA401286555

Gene: TIMP2

Linked Data

• gnomAD v4: 17-78870901-C-A
• MyVariant Identifiers: chr17:g.76866983C>A (hg19) ; chr17:g.78870901C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.78870901C>A , CM000679.2:g.78870901C>A	GRCh38
NC_000017.10:g.76866983C>A , CM000679.1:g.76866983C>A	GRCh37
NC_000017.9:g.74378578C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586713.6:c.106G>T	ENSP00000465968.2:p.Ala36Ser
ENST00000706922.1:c.106G>T	ENSP00000516642.1:p.Ala36Ser
ENST00000706923.1:c.106G>T	ENSP00000516643.1:p.Ala36Ser
ENST00000262768.11:c.337G>T MANE Select	ENSP00000262768.6:p.Ala113Ser
ENST00000536189.6:c.106G>T	ENSP00000441724.1:p.Ala36Ser
ENST00000585421.5:c.106G>T	ENSP00000467584.1:p.Ala36Ser
ENST00000586057.5:c.106G>T	ENSP00000468296.1:p.Ala36Ser
ENST00000592761.2:c.106G>T	ENSP00000464930.1:p.Ala36Ser
NM_003255.4:c.337G>T	NP_003246.1:p.Ala113Ser
NM_003255.5:c.337G>T MANE Select	NP_003246.1:p.Ala113Ser