Canonical Allele Identifier: CA2624150834
Gene: MMP14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843525_22843538del , CM000676.2:g.22843525_22843538del GRCh38
NC_000014.8:g.23312734_23312747del , CM000676.1:g.23312734_23312747del GRCh37
NC_000014.7:g.22382574_22382587del NCBI36
NG_046989.1:g.11993_12006del

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.850+107_850+120del MANE Select ENSP00000308208.6:n.850+107_850+120del
ENST00000548162.2:c.850+107_850+120del ENSP00000506068.1:n.850+107_850+120del
ENST00000680097.1:c.*165+107_*165+120del ENSP00000506631.1:n.*165+107_*165+120del
ENST00000680941.1:c.*248+107_*248+120del ENSP00000506378.1:n.*248+107_*248+120del
ENST00000311852.10:c.850+107_850+120del ENSP00000308208.6:n.850+107_850+120del
ENST00000548162.1:n.1092+107_1092+120del
NM_004995.3:c.850+107_850+120del NP_004986.1:n.850+107_850+120del
NM_004995.4:c.850+107_850+120del MANE Select NP_004986.1:n.850+107_850+120del