Canonical Allele Identifier: CA2123185443
Gene: MMP14 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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