Canonical Allele Identifier: CA2123185365

Gene: MMP14

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22843466_22843467delinsCT , CM000676.2:g.22843466_22843467delinsCT	GRCh38
NC_000014.8:g.23312675_23312676delinsCT , CM000676.1:g.23312675_23312676delinsCT	GRCh37
NC_000014.7:g.22382515_22382516delinsCT	NCBI36
NG_046989.1:g.11934_11935delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311852.11:c.850+48_850+49delinsCT MANE Select	ENSP00000308208.6:n.850+48_850+49delinsCT
ENST00000548162.2:c.850+48_850+49delinsCT	ENSP00000506068.1:n.850+48_850+49delinsCT
ENST00000680097.1:c.*165+48_*165+49delinsCT	ENSP00000506631.1:n.*165+48_*165+49delinsCT
ENST00000680941.1:c.*248+48_*248+49delinsCT	ENSP00000506378.1:n.*248+48_*248+49delinsCT
ENST00000311852.10:c.850+48_850+49delinsCT	ENSP00000308208.6:n.850+48_850+49delinsCT
ENST00000548162.1:n.1092+48_1092+49delinsCT
NM_004995.3:c.850+48_850+49delinsCT	NP_004986.1:n.850+48_850+49delinsCT
NM_004995.4:c.850+48_850+49delinsCT MANE Select	NP_004986.1:n.850+48_850+49delinsCT