Canonical Allele Identifier: CA601246157
Gene: WTAPP1 HGNC NCBI
MMP1 HGNC NCBI

Linked Data

dbSNP Id: rs1466376722
gnomAD v2: 11-102668965-C-T
gnomAD v4: 11-102798234-C-T
MyVariant Identifiers: chr11:g.102668965C>T (hg19) chr11:g.102798234C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798234C>T , CM000673.2:g.102798234C>T GRCh38
NC_000011.9:g.102668965C>T , CM000673.1:g.102668965C>T GRCh37
NC_000011.8:g.102174175C>T NCBI36
NG_011740.1:g.5002G>A
NG_011740.2:g.5002G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+112C>T (WTAPP1)
ENST00000525739.6:n.682+112C>T (WTAPP1)
ENST00000544704.1:n.443+112C>T (WTAPP1)
NM_001145938.1:c.-188G>A (MMP1) NP_001139410.1:n.-188G>A
NM_002421.3:c.-142G>A (MMP1) NP_002412.1:n.-142G>A
NR_038390.1:n.682+112C>T (WTAPP1)
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