Canonical Allele Identifier: CA2123185379

Gene: MMP14

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22843486_22843488delinsCCT , CM000676.2:g.22843486_22843488delinsCCT	GRCh38
NC_000014.8:g.23312695_23312697delinsCCT , CM000676.1:g.23312695_23312697delinsCCT	GRCh37
NC_000014.7:g.22382535_22382537delinsCCT	NCBI36
NG_046989.1:g.11954_11956delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311852.11:c.850+68_850+70delinsCCT MANE Select	ENSP00000308208.6:n.850+68_850+70delinsCCT
ENST00000548162.2:c.850+68_850+70delinsCCT	ENSP00000506068.1:n.850+68_850+70delinsCCT
ENST00000680097.1:c.*165+68_*165+70delinsCCT	ENSP00000506631.1:n.*165+68_*165+70delinsCCT
ENST00000680941.1:c.*248+68_*248+70delinsCCT	ENSP00000506378.1:n.*248+68_*248+70delinsCCT
ENST00000311852.10:c.850+68_850+70delinsCCT	ENSP00000308208.6:n.850+68_850+70delinsCCT
ENST00000548162.1:n.1092+68_1092+70delinsCCT
NM_004995.3:c.850+68_850+70delinsCCT	NP_004986.1:n.850+68_850+70delinsCCT
NM_004995.4:c.850+68_850+70delinsCCT MANE Select	NP_004986.1:n.850+68_850+70delinsCCT