Canonical Allele Identifier: CA2123185452
Gene: MMP14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843615C= , CM000676.2:g.22843615C= GRCh38
NC_000014.8:g.23312824C= , CM000676.1:g.23312824C= GRCh37
NC_000014.7:g.22382664C= NCBI36
NG_046989.1:g.12083C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.851-95C= MANE Select ENSP00000308208.6:n.851-95C=
ENST00000548162.2:c.851-95C= ENSP00000506068.1:n.851-95C=
ENST00000680097.1:c.*166-95C= ENSP00000506631.1:n.*166-95C=
ENST00000680941.1:c.*249-95C= ENSP00000506378.1:n.*249-95C=
ENST00000311852.10:c.851-95C= ENSP00000308208.6:n.851-95C=
ENST00000548162.1:n.1093-95C=
NM_004995.3:c.851-95C= NP_004986.1:n.851-95C=
NM_004995.4:c.851-95C= MANE Select NP_004986.1:n.851-95C=