Canonical Allele Identifier: CA382226456

Gene: MMP1 WTAPP1

Linked Data

• MyVariant Identifiers: chr11:g.102661169T>G (hg19) ; chr11:g.102790438T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102790438T>G , CM000673.2:g.102790438T>G	GRCh38
NC_000011.9:g.102661169T>G , CM000673.1:g.102661169T>G	GRCh37
NC_000011.8:g.102166379T>G	NCBI36
NG_011740.1:g.12798A>C
NG_011740.2:g.12798A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315274.7:c.1384A>C (MMP1) MANE Select	ENSP00000322788.6:p.Ser462Arg
ENST00000680179.1:n.562A>C (MMP1)
ENST00000681445.1:n.558A>C (MMP1)
ENST00000681643.1:n.584A>C (MMP1)
ENST00000315274.6:c.1384A>C (MMP1)	ENSP00000322788.6:p.Ser462Arg
ENST00000371455.7:n.325-7586T>G (WTAPP1)
ENST00000525739.6:n.390-2707T>G (WTAPP1)
ENST00000544704.1:n.344+6374T>G (WTAPP1)
NM_001145938.1:c.1186A>C (MMP1)	NP_001139410.1:p.Ser396Arg
NM_002421.3:c.1384A>C (MMP1)	NP_002412.1:p.Ser462Arg
NR_038390.1:n.390-2707T>G (WTAPP1)
NM_002421.4:c.1384A>C (MMP1) MANE Select	NP_002412.1:p.Ser462Arg
NM_001145938.2:c.1186A>C (MMP1)	NP_001139410.1:p.Ser396Arg