Canonical Allele Identifier: CA382209698

Gene: MMP7

Linked Data

• MyVariant Identifiers: chr11:g.102398527G>A (hg19) ; chr11:g.102527796G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102527796G>A , CM000673.2:g.102527796G>A	GRCh38
NC_000011.9:g.102398527G>A , CM000673.1:g.102398527G>A	GRCh37
NC_000011.8:g.101903737G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260227.5:c.296C>T MANE Select	ENSP00000260227.4:p.Pro99Leu
ENST00000260227.4:c.296C>T	ENSP00000260227.4:p.Pro99Leu
ENST00000531200.1:n.343C>T
ENST00000533366.5:n.346C>T
NM_002423.3:c.296C>T	NP_002414.1:p.Pro99Leu
NM_002423.4:c.296C>T	NP_002414.1:p.Pro99Leu
NM_002423.5:c.296C>T MANE Select	NP_002414.1:p.Pro99Leu