Canonical Allele Identifier: CA2123185217
Gene: MMP14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843066C= , CM000676.2:g.22843066C= GRCh38
NC_000014.8:g.23312275C= , CM000676.1:g.23312275C= GRCh37
NC_000014.7:g.22382115C= NCBI36
NG_046989.1:g.11534C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.689-191C= MANE Select ENSP00000308208.6:n.689-191C=
ENST00000548162.2:c.689-191C= ENSP00000506068.1:n.689-191C=
ENST00000680097.1:c.*4-191C= ENSP00000506631.1:n.*4-191C=
ENST00000680941.1:c.733C= ENSP00000506378.1:p.Pro245=
ENST00000311852.10:c.689-191C= ENSP00000308208.6:n.689-191C=
ENST00000548162.1:n.931-191C=
NM_004995.3:c.689-191C= NP_004986.1:n.689-191C=
NM_004995.4:c.689-191C= MANE Select NP_004986.1:n.689-191C=
Search 100 bp 5'
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