Canonical Allele Identifier: CA2615724678

Gene: MMP1 WTAPP1

Linked Data

• gnomAD v4: 11-102790140-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790140T>A , CM000673.2:g.102790140T>A	GRCh38
NC_000011.9:g.102660871T>A , CM000673.1:g.102660871T>A	GRCh37
NC_000011.8:g.102166081T>A	NCBI36
NG_011740.1:g.13096A>T
NG_011740.2:g.13096A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315274.7:c.*272A>T (MMP1) MANE Select	ENSP00000322788.6:n.*272A>T
ENST00000680179.1:n.860A>T (MMP1)
ENST00000681445.1:n.856A>T (MMP1)
ENST00000681643.1:n.882A>T (MMP1)
ENST00000315274.6:c.*272A>T (MMP1)	ENSP00000322788.6:n.*272A>T
ENST00000371455.7:n.325-7884T>A (WTAPP1)
ENST00000525739.6:n.390-3005T>A (WTAPP1)
ENST00000544704.1:n.344+6076T>A (WTAPP1)
NM_001145938.1:c.*272A>T (MMP1)	NP_001139410.1:n.*272A>T
NM_002421.3:c.*272A>T (MMP1)	NP_002412.1:n.*272A>T
NR_038390.1:n.390-3005T>A (WTAPP1)
NM_002421.4:c.*272A>T (MMP1) MANE Select	NP_002412.1:n.*272A>T
NM_001145938.2:c.*272A>T (MMP1)	NP_001139410.1:n.*272A>T