Canonical Allele Identifier: CA2615724587

Gene: MMP1 WTAPP1

Linked Data

• gnomAD v4: 11-102790109-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790109G>A , CM000673.2:g.102790109G>A	GRCh38
NC_000011.9:g.102660840G>A , CM000673.1:g.102660840G>A	GRCh37
NC_000011.8:g.102166050G>A	NCBI36
NG_011740.1:g.13127C>T
NG_011740.2:g.13127C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315274.7:c.*303C>T (MMP1) MANE Select	ENSP00000322788.6:n.*303C>T
ENST00000680179.1:n.891C>T (MMP1)
ENST00000681445.1:n.887C>T (MMP1)
ENST00000681643.1:n.913C>T (MMP1)
ENST00000315274.6:c.*303C>T (MMP1)	ENSP00000322788.6:n.*303C>T
ENST00000371455.7:n.325-7915G>A (WTAPP1)
ENST00000525739.6:n.390-3036G>A (WTAPP1)
ENST00000544704.1:n.344+6045G>A (WTAPP1)
NM_001145938.1:c.*303C>T (MMP1)	NP_001139410.1:n.*303C>T
NM_002421.3:c.*303C>T (MMP1)	NP_002412.1:n.*303C>T
NR_038390.1:n.390-3036G>A (WTAPP1)
NM_002421.4:c.*303C>T (MMP1) MANE Select	NP_002412.1:n.*303C>T
NM_001145938.2:c.*303C>T (MMP1)	NP_001139410.1:n.*303C>T