Canonical Allele Identifier: CA382226794

Gene: MMP1 WTAPP1

Linked Data

• MyVariant Identifiers: chr11:g.102661496T>A (hg19) ; chr11:g.102790765T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790765T>A , CM000673.2:g.102790765T>A	GRCh38
NC_000011.9:g.102661496T>A , CM000673.1:g.102661496T>A	GRCh37
NC_000011.8:g.102166706T>A	NCBI36
NG_011740.1:g.12471A>T
NG_011740.2:g.12471A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000315274.7:c.1238A>T (MMP1) MANE Select	ENSP00000322788.6:p.Lys413Ile
ENST00000680179.1:n.416A>T (MMP1)
ENST00000681445.1:n.412A>T (MMP1)
ENST00000681643.1:n.438A>T (MMP1)
ENST00000315274.6:c.1238A>T (MMP1)	ENSP00000322788.6:p.Lys413Ile
ENST00000371455.7:n.325-7259T>A (WTAPP1)
ENST00000525739.6:n.390-2380T>A (WTAPP1)
ENST00000544704.1:n.344+6701T>A (WTAPP1)
NM_001145938.1:c.1040A>T (MMP1)	NP_001139410.1:p.Lys347Ile
NM_002421.3:c.1238A>T (MMP1)	NP_002412.1:p.Lys413Ile
NR_038390.1:n.390-2380T>A (WTAPP1)
NM_002421.4:c.1238A>T (MMP1) MANE Select	NP_002412.1:p.Lys413Ile
NM_001145938.2:c.1040A>T (MMP1)	NP_001139410.1:p.Lys347Ile