Canonical Allele Identifier: CA227360218

Gene: MMP1 WTAPP1

Linked Data

• dbSNP Id: rs776054089
• gnomAD v4: 11-102790296-A-T
• MyVariant Identifiers: chr11:g.102661027A>T (hg19) ; chr11:g.102790296A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790296A>T , CM000673.2:g.102790296A>T	GRCh38
NC_000011.9:g.102661027A>T , CM000673.1:g.102661027A>T	GRCh37
NC_000011.8:g.102166237A>T	NCBI36
NG_011740.1:g.12940T>A
NG_011740.2:g.12940T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315274.7:c.*116T>A (MMP1) MANE Select	ENSP00000322788.6:n.*116T>A
ENST00000680179.1:n.704T>A (MMP1)
ENST00000681445.1:n.700T>A (MMP1)
ENST00000681643.1:n.726T>A (MMP1)
ENST00000315274.6:c.*116T>A (MMP1)	ENSP00000322788.6:n.*116T>A
ENST00000371455.7:n.325-7728A>T (WTAPP1)
ENST00000525739.6:n.390-2849A>T (WTAPP1)
ENST00000544704.1:n.344+6232A>T (WTAPP1)
NM_001145938.1:c.*116T>A (MMP1)	NP_001139410.1:n.*116T>A
NM_002421.3:c.*116T>A (MMP1)	NP_002412.1:n.*116T>A
NR_038390.1:n.390-2849A>T (WTAPP1)
NM_002421.4:c.*116T>A (MMP1) MANE Select	NP_002412.1:n.*116T>A
NM_001145938.2:c.*116T>A (MMP1)	NP_001139410.1:n.*116T>A