Canonical Allele Identifier: CA2123185442
Gene: MMP14 HGNC NCBI

Linked Data

dbSNP Id: rs2039789004
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843598C>G , CM000676.2:g.22843598C>G GRCh38
NC_000014.8:g.23312807C>G , CM000676.1:g.23312807C>G GRCh37
NC_000014.7:g.22382647C>G NCBI36
NG_046989.1:g.12066C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.851-112C>G MANE Select ENSP00000308208.6:n.851-112C>G
ENST00000548162.2:c.851-112C>G ENSP00000506068.1:n.851-112C>G
ENST00000680097.1:c.*166-112C>G ENSP00000506631.1:n.*166-112C>G
ENST00000680941.1:c.*249-112C>G ENSP00000506378.1:n.*249-112C>G
ENST00000311852.10:c.851-112C>G ENSP00000308208.6:n.851-112C>G
ENST00000548162.1:n.1093-112C>G
NM_004995.3:c.851-112C>G NP_004986.1:n.851-112C>G
NM_004995.4:c.851-112C>G MANE Select NP_004986.1:n.851-112C>G
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