Canonical Allele Identifier: CA2624150942
Gene: MMP14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843622_22843643dup , CM000676.2:g.22843622_22843643dup GRCh38
NC_000014.8:g.23312831_23312852dup , CM000676.1:g.23312831_23312852dup GRCh37
NC_000014.7:g.22382671_22382692dup NCBI36
NG_046989.1:g.12090_12111dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.851-88_851-67dup MANE Select ENSP00000308208.6:n.851-88_851-67dup
ENST00000548162.2:c.851-88_851-67dup ENSP00000506068.1:n.851-88_851-67dup
ENST00000680097.1:c.*166-88_*166-67dup ENSP00000506631.1:n.*166-88_*166-67dup
ENST00000680941.1:c.*249-88_*249-67dup ENSP00000506378.1:n.*249-88_*249-67dup
ENST00000311852.10:c.851-88_851-67dup ENSP00000308208.6:n.851-88_851-67dup
ENST00000548162.1:n.1093-88_1093-67dup
NM_004995.3:c.851-88_851-67dup NP_004986.1:n.851-88_851-67dup
NM_004995.4:c.851-88_851-67dup MANE Select NP_004986.1:n.851-88_851-67dup