Canonical Allele Identifier: CA2123185369

Gene: MMP14

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22843470_22843471delinsTG , CM000676.2:g.22843470_22843471delinsTG	GRCh38
NC_000014.8:g.23312679_23312680delinsTG , CM000676.1:g.23312679_23312680delinsTG	GRCh37
NC_000014.7:g.22382519_22382520delinsTG	NCBI36
NG_046989.1:g.11938_11939delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311852.11:c.850+52_850+53delinsTG MANE Select	ENSP00000308208.6:n.850+52_850+53delinsTG
ENST00000548162.2:c.850+52_850+53delinsTG	ENSP00000506068.1:n.850+52_850+53delinsTG
ENST00000680097.1:c.*165+52_*165+53delinsTG	ENSP00000506631.1:n.*165+52_*165+53delinsTG
ENST00000680941.1:c.*248+52_*248+53delinsTG	ENSP00000506378.1:n.*248+52_*248+53delinsTG
ENST00000311852.10:c.850+52_850+53delinsTG	ENSP00000308208.6:n.850+52_850+53delinsTG
ENST00000548162.1:n.1092+52_1092+53delinsTG
NM_004995.3:c.850+52_850+53delinsTG	NP_004986.1:n.850+52_850+53delinsTG
NM_004995.4:c.850+52_850+53delinsTG MANE Select	NP_004986.1:n.850+52_850+53delinsTG