Canonical Allele Identifier: CA6250181
Gene: MMP10 HGNC NCBI
WTAPP1 HGNC NCBI

Linked Data

dbSNP Id: rs17293607
ExAC: 11:102650389 C / T
gnomAD v2: 11-102650389-C-T
gnomAD v3: 11-102779658-C-T
gnomAD v4: 11-102779658-C-T
MyVariant Identifiers: chr11:g.102650389C>T (hg19) chr11:g.102779658C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.102779658C>T , CM000673.2:g.102779658C>T GRCh38
NC_000011.9:g.102650389C>T , CM000673.1:g.102650389C>T GRCh37
NC_000011.8:g.102155599C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000279441.9:c.193G>A (MMP10) MANE Select ENSP00000279441.4:p.Gly65Arg
ENST00000279441.8:c.193G>A (MMP10) ENSP00000279441.4:p.Gly65Arg
ENST00000371455.7:n.325-18366C>T (WTAPP1)
ENST00000539681.1:c.193G>A (MMP10) ENSP00000441485.1:p.Gly65Arg
NM_002425.2:c.193G>A (MMP10) NP_002416.1:p.Gly65Arg
NM_002425.3:c.193G>A (MMP10) MANE Select NP_002416.1:p.Gly65Arg
Search 100 bp 5'
Search 100 bp 3'