Canonical Allele Identifier: CA2123185226
Gene: MMP14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843085G= , CM000676.2:g.22843085G= GRCh38
NC_000014.8:g.23312294G= , CM000676.1:g.23312294G= GRCh37
NC_000014.7:g.22382134G= NCBI36
NG_046989.1:g.11553G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.689-172G= MANE Select ENSP00000308208.6:n.689-172G=
ENST00000548162.2:c.689-172G= ENSP00000506068.1:n.689-172G=
ENST00000680097.1:c.*4-172G= ENSP00000506631.1:n.*4-172G=
ENST00000680941.1:c.752G= ENSP00000506378.1:p.Ter251=
ENST00000311852.10:c.689-172G= ENSP00000308208.6:n.689-172G=
ENST00000548162.1:n.931-172G=
NM_004995.3:c.689-172G= NP_004986.1:n.689-172G=
NM_004995.4:c.689-172G= MANE Select NP_004986.1:n.689-172G=
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