Canonical Allele Identifier: CA382226712

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790730T>A , CM000673.2:g.102790730T>A GRCh38
NC_000011.9:g.102661461T>A , CM000673.1:g.102661461T>A GRCh37
NC_000011.8:g.102166671T>A NCBI36
NG_011740.1:g.12506A>T
NG_011740.2:g.12506A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315274.7:c.1273A>T (MMP1) MANE Select ENSP00000322788.6:p.Lys425Ter
ENST00000680179.1:n.451A>T (MMP1)
ENST00000681445.1:n.447A>T (MMP1)
ENST00000681643.1:n.473A>T (MMP1)
ENST00000315274.6:c.1273A>T (MMP1) ENSP00000322788.6:p.Lys425Ter
ENST00000371455.7:n.325-7294T>A (WTAPP1)
ENST00000525739.6:n.390-2415T>A (WTAPP1)
ENST00000544704.1:n.344+6666T>A (WTAPP1)
NM_001145938.1:c.1075A>T (MMP1) NP_001139410.1:p.Lys359Ter
NM_002421.3:c.1273A>T (MMP1) NP_002412.1:p.Lys425Ter
NR_038390.1:n.390-2415T>A (WTAPP1)
NM_002421.4:c.1273A>T (MMP1) MANE Select NP_002412.1:p.Lys425Ter
NM_001145938.2:c.1075A>T (MMP1) NP_001139410.1:p.Lys359Ter