Canonical Allele Identifier: CA2624150750

Gene: MMP14

Linked Data

• gnomAD v4: 14-22843225-GGCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22843229_22843231del , CM000676.2:g.22843229_22843231del	GRCh38
NC_000014.8:g.23312438_23312440del , CM000676.1:g.23312438_23312440del	GRCh37
NC_000014.7:g.22382278_22382280del	NCBI36
NG_046989.1:g.11697_11699del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311852.11:c.689-28_689-26del MANE Select	ENSP00000308208.6:n.689-28_689-26del
ENST00000548162.2:c.689-28_689-26del	ENSP00000506068.1:n.689-28_689-26del
ENST00000680097.1:c.*4-28_*4-26del	ENSP00000506631.1:n.*4-28_*4-26del
ENST00000680941.1:c.*87-28_*87-26del	ENSP00000506378.1:n.*87-28_*87-26del
ENST00000311852.10:c.689-28_689-26del	ENSP00000308208.6:n.689-28_689-26del
ENST00000548162.1:n.931-28_931-26del
NM_004995.3:c.689-28_689-26del	NP_004986.1:n.689-28_689-26del
NM_004995.4:c.689-28_689-26del MANE Select	NP_004986.1:n.689-28_689-26del