Canonical Allele Identifier: CA476737592

Linked Data

MyVariant Identifiers: chr11:g.102661480G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790749G>A , CM000673.2:g.102790749G>A GRCh38
NC_000011.9:g.102661480G>A , CM000673.1:g.102661480G>A GRCh37
NC_000011.8:g.102166690G>A NCBI36
NG_011740.1:g.12487C>T
NG_011740.2:g.12487C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315274.7:c.1254C>T (MMP1) MANE Select ENSP00000322788.6:p.Asp418=
ENST00000680179.1:n.432C>T (MMP1)
ENST00000681445.1:n.428C>T (MMP1)
ENST00000681643.1:n.454C>T (MMP1)
ENST00000315274.6:c.1254C>T (MMP1) ENSP00000322788.6:p.Asp418=
ENST00000371455.7:n.325-7275G>A (WTAPP1)
ENST00000525739.6:n.390-2396G>A (WTAPP1)
ENST00000544704.1:n.344+6685G>A (WTAPP1)
NM_001145938.1:c.1056C>T (MMP1) NP_001139410.1:p.Asp352=
NM_002421.3:c.1254C>T (MMP1) NP_002412.1:p.Asp418=
NR_038390.1:n.390-2396G>A (WTAPP1)
NM_002421.4:c.1254C>T (MMP1) MANE Select NP_002412.1:p.Asp418=
NM_001145938.2:c.1056C>T (MMP1) NP_001139410.1:p.Asp352=