Canonical Allele Identifier: CA2615726059

Gene: MMP1 WTAPP1

Linked Data

• gnomAD v4: 11-102790953-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790953G>T , CM000673.2:g.102790953G>T	GRCh38
NC_000011.9:g.102661684G>T , CM000673.1:g.102661684G>T	GRCh37
NC_000011.8:g.102166894G>T	NCBI36
NG_011740.1:g.12283C>A
NG_011740.2:g.12283C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000315274.7:c.1197-147C>A (MMP1) MANE Select	ENSP00000322788.6:n.1197-147C>A
ENST00000680179.1:n.375-147C>A (MMP1)
ENST00000681445.1:n.371-147C>A (MMP1)
ENST00000681643.1:n.397-147C>A (MMP1)
ENST00000315274.6:c.1197-147C>A (MMP1)	ENSP00000322788.6:n.1197-147C>A
ENST00000371455.7:n.325-7071G>T (WTAPP1)
ENST00000525739.6:n.390-2192G>T (WTAPP1)
ENST00000544704.1:n.344+6889G>T (WTAPP1)
NM_001145938.1:c.999-147C>A (MMP1)	NP_001139410.1:n.999-147C>A
NM_002421.3:c.1197-147C>A (MMP1)	NP_002412.1:n.1197-147C>A
NR_038390.1:n.390-2192G>T (WTAPP1)
NM_002421.4:c.1197-147C>A (MMP1) MANE Select	NP_002412.1:n.1197-147C>A
NM_001145938.2:c.999-147C>A (MMP1)	NP_001139410.1:n.999-147C>A