Canonical Allele Identifier: CA961019781
Gene: MMP14 HGNC NCBI

Linked Data

dbSNP Id: rs2039788929
gnomAD v3: 14-22843578-T-A
gnomAD v4: 14-22843578-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843578T>A , CM000676.2:g.22843578T>A GRCh38
NC_000014.8:g.23312787T>A , CM000676.1:g.23312787T>A GRCh37
NC_000014.7:g.22382627T>A NCBI36
NG_046989.1:g.12046T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.851-132T>A MANE Select ENSP00000308208.6:n.851-132T>A
ENST00000548162.2:c.851-132T>A ENSP00000506068.1:n.851-132T>A
ENST00000680097.1:c.*166-132T>A ENSP00000506631.1:n.*166-132T>A
ENST00000680941.1:c.*249-132T>A ENSP00000506378.1:n.*249-132T>A
ENST00000311852.10:c.851-132T>A ENSP00000308208.6:n.851-132T>A
ENST00000548162.1:n.1093-132T>A
NM_004995.3:c.851-132T>A NP_004986.1:n.851-132T>A
NM_004995.4:c.851-132T>A MANE Select NP_004986.1:n.851-132T>A
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