Canonical Allele Identifier: CA670876231
Gene: WTAPP1 HGNC NCBI
MMP1 HGNC NCBI

Linked Data

dbSNP Id: rs1366555839
gnomAD v4: 11-102798200-C-A
MyVariant Identifiers: chr11:g.102668931C>A (hg19) chr11:g.102798200C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102798200C>A , CM000673.2:g.102798200C>A GRCh38
NC_000011.9:g.102668931C>A , CM000673.1:g.102668931C>A GRCh37
NC_000011.8:g.102174141C>A NCBI36
NG_011740.1:g.5036G>T
NG_011740.2:g.5036G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371455.7:n.423+78C>A (WTAPP1)
ENST00000525739.6:n.682+78C>A (WTAPP1)
ENST00000544704.1:n.443+78C>A (WTAPP1)
NM_001145938.1:c.-154G>T (MMP1) NP_001139410.1:n.-154G>T
NM_002421.3:c.-108G>T (MMP1) NP_002412.1:n.-108G>T
NR_038390.1:n.682+78C>A (WTAPP1)
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