Canonical Allele Identifier: CA961019791
Gene: MMP14 HGNC NCBI

Linked Data

dbSNP Id: rs1847024833
gnomAD v3: 14-22843627-A-G
gnomAD v4: 14-22843627-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843627A>G , CM000676.2:g.22843627A>G GRCh38
NC_000014.8:g.23312836A>G , CM000676.1:g.23312836A>G GRCh37
NC_000014.7:g.22382676A>G NCBI36
NG_046989.1:g.12095A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.851-83A>G MANE Select ENSP00000308208.6:n.851-83A>G
ENST00000548162.2:c.851-83A>G ENSP00000506068.1:n.851-83A>G
ENST00000680097.1:c.*166-83A>G ENSP00000506631.1:n.*166-83A>G
ENST00000680941.1:c.*249-83A>G ENSP00000506378.1:n.*249-83A>G
ENST00000311852.10:c.851-83A>G ENSP00000308208.6:n.851-83A>G
ENST00000548162.1:n.1093-83A>G
NM_004995.3:c.851-83A>G NP_004986.1:n.851-83A>G
NM_004995.4:c.851-83A>G MANE Select NP_004986.1:n.851-83A>G
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Search 100 bp 3'