Canonical Allele Identifier: CA2615724594

Gene: MMP1 WTAPP1

Linked Data

• gnomAD v4: 11-102790114-C-CGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790114_102790115insGG , CM000673.2:g.102790114_102790115insGG	GRCh38
NC_000011.9:g.102660845_102660846insGG , CM000673.1:g.102660845_102660846insGG	GRCh37
NC_000011.8:g.102166055_102166056insGG	NCBI36
NG_011740.1:g.13121_13122insCC
NG_011740.2:g.13121_13122insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315274.7:c.*297_*298insCC (MMP1) MANE Select	ENSP00000322788.6:n.*297_*298insCC
ENST00000680179.1:n.885_886insCC (MMP1)
ENST00000681445.1:n.881_882insCC (MMP1)
ENST00000681643.1:n.907_908insCC (MMP1)
ENST00000315274.6:c.*297_*298insCC (MMP1)	ENSP00000322788.6:n.*297_*298insCC
ENST00000371455.7:n.325-7910_325-7909insGG (WTAPP1)
ENST00000525739.6:n.390-3031_390-3030insGG (WTAPP1)
ENST00000544704.1:n.344+6050_344+6051insGG (WTAPP1)
NM_001145938.1:c.*297_*298insCC (MMP1)	NP_001139410.1:n.*297_*298insCC
NM_002421.3:c.*297_*298insCC (MMP1)	NP_002412.1:n.*297_*298insCC
NR_038390.1:n.390-3031_390-3030insGG (WTAPP1)
NM_002421.4:c.*297_*298insCC (MMP1) MANE Select	NP_002412.1:n.*297_*298insCC
NM_001145938.2:c.*297_*298insCC (MMP1)	NP_001139410.1:n.*297_*298insCC