Canonical Allele Identifier: CA2624150885
Gene: MMP14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843551_22843552insGCCCAT , CM000676.2:g.22843551_22843552insGCCCAT GRCh38
NC_000014.8:g.23312760_23312761insGCCCAT , CM000676.1:g.23312760_23312761insGCCCAT GRCh37
NC_000014.7:g.22382600_22382601insGCCCAT NCBI36
NG_046989.1:g.12019_12020insGCCCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.850+133_850+134insGCCCAT MANE Select ENSP00000308208.6:n.850+133_850+134insGCCCAT
ENST00000548162.2:c.850+133_850+134insGCCCAT ENSP00000506068.1:n.850+133_850+134insGCCCAT
ENST00000680097.1:c.*165+133_*165+134insGCCCAT ENSP00000506631.1:n.*165+133_*165+134insGCCCAT
ENST00000680941.1:c.*248+133_*248+134insGCCCAT ENSP00000506378.1:n.*248+133_*248+134insGCCCAT
ENST00000311852.10:c.850+133_850+134insGCCCAT ENSP00000308208.6:n.850+133_850+134insGCCCAT
ENST00000548162.1:n.1092+133_1092+134insGCCCAT
NM_004995.3:c.850+133_850+134insGCCCAT NP_004986.1:n.850+133_850+134insGCCCAT
NM_004995.4:c.850+133_850+134insGCCCAT MANE Select NP_004986.1:n.850+133_850+134insGCCCAT