Canonical Allele Identifier: CA382209995

Gene: MMP7

Linked Data

• MyVariant Identifiers: chr11:g.102398560C>A (hg19) ; chr11:g.102527829C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102527829C>A , CM000673.2:g.102527829C>A	GRCh38
NC_000011.9:g.102398560C>A , CM000673.1:g.102398560C>A	GRCh37
NC_000011.8:g.101903770C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260227.5:c.263G>T MANE Select	ENSP00000260227.4:p.Gly88Val
ENST00000260227.4:c.263G>T	ENSP00000260227.4:p.Gly88Val
ENST00000531200.1:n.310G>T
ENST00000533366.5:n.313G>T
NM_002423.3:c.263G>T	NP_002414.1:p.Gly88Val
NM_002423.4:c.263G>T	NP_002414.1:p.Gly88Val
NM_002423.5:c.263G>T MANE Select	NP_002414.1:p.Gly88Val