Canonical Allele Identifier: CA2123185242
Gene: MMP14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843123C= , CM000676.2:g.22843123C= GRCh38
NC_000014.8:g.23312332C= , CM000676.1:g.23312332C= GRCh37
NC_000014.7:g.22382172C= NCBI36
NG_046989.1:g.11591C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.689-134C= MANE Select ENSP00000308208.6:n.689-134C=
ENST00000548162.2:c.689-134C= ENSP00000506068.1:n.689-134C=
ENST00000680097.1:c.*4-134C= ENSP00000506631.1:n.*4-134C=
ENST00000680941.1:c.*37C= ENSP00000506378.1:n.*37C=
ENST00000311852.10:c.689-134C= ENSP00000308208.6:n.689-134C=
ENST00000548162.1:n.931-134C=
NM_004995.3:c.689-134C= NP_004986.1:n.689-134C=
NM_004995.4:c.689-134C= MANE Select NP_004986.1:n.689-134C=
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