Canonical Allele Identifier: CA2602012907

Linked Data

dbSNP Id: rs2134359896

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102790131G>A , CM000673.2:g.102790131G>A GRCh38
NC_000011.9:g.102660862G>A , CM000673.1:g.102660862G>A GRCh37
NC_000011.8:g.102166072G>A NCBI36
NG_011740.1:g.13105C>T
NG_011740.2:g.13105C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000315274.7:c.*281C>T (MMP1) MANE Select ENSP00000322788.6:n.*281C>T
ENST00000680179.1:n.869C>T (MMP1)
ENST00000681445.1:n.865C>T (MMP1)
ENST00000681643.1:n.891C>T (MMP1)
ENST00000315274.6:c.*281C>T (MMP1) ENSP00000322788.6:n.*281C>T
ENST00000371455.7:n.325-7893G>A (WTAPP1)
ENST00000525739.6:n.390-3014G>A (WTAPP1)
ENST00000544704.1:n.344+6067G>A (WTAPP1)
NM_001145938.1:c.*281C>T (MMP1) NP_001139410.1:n.*281C>T
NM_002421.3:c.*281C>T (MMP1) NP_002412.1:n.*281C>T
NR_038390.1:n.390-3014G>A (WTAPP1)
NM_002421.4:c.*281C>T (MMP1) MANE Select NP_002412.1:n.*281C>T
NM_001145938.2:c.*281C>T (MMP1) NP_001139410.1:n.*281C>T