Canonical Allele Identifier: CA476737586

Linked Data

MyVariant Identifiers: chr11:g.102661468A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790737A>T , CM000673.2:g.102790737A>T GRCh38
NC_000011.9:g.102661468A>T , CM000673.1:g.102661468A>T GRCh37
NC_000011.8:g.102166678A>T NCBI36
NG_011740.1:g.12499T>A
NG_011740.2:g.12499T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315274.7:c.1266T>A (MMP1) MANE Select ENSP00000322788.6:p.Ile422=
ENST00000680179.1:n.444T>A (MMP1)
ENST00000681445.1:n.440T>A (MMP1)
ENST00000681643.1:n.466T>A (MMP1)
ENST00000315274.6:c.1266T>A (MMP1) ENSP00000322788.6:p.Ile422=
ENST00000371455.7:n.325-7287A>T (WTAPP1)
ENST00000525739.6:n.390-2408A>T (WTAPP1)
ENST00000544704.1:n.344+6673A>T (WTAPP1)
NM_001145938.1:c.1068T>A (MMP1) NP_001139410.1:p.Ile356=
NM_002421.3:c.1266T>A (MMP1) NP_002412.1:p.Ile422=
NR_038390.1:n.390-2408A>T (WTAPP1)
NM_002421.4:c.1266T>A (MMP1) MANE Select NP_002412.1:p.Ile422=
NM_001145938.2:c.1068T>A (MMP1) NP_001139410.1:p.Ile356=