Canonical Allele Identifier: CA2624150791

Gene: MMP14

Linked Data

• gnomAD v4: 14-22843465-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22843465C>T , CM000676.2:g.22843465C>T	GRCh38
NC_000014.8:g.23312674C>T , CM000676.1:g.23312674C>T	GRCh37
NC_000014.7:g.22382514C>T	NCBI36
NG_046989.1:g.11933C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311852.11:c.850+47C>T MANE Select	ENSP00000308208.6:n.850+47C>T
ENST00000548162.2:c.850+47C>T	ENSP00000506068.1:n.850+47C>T
ENST00000680097.1:c.*165+47C>T	ENSP00000506631.1:n.*165+47C>T
ENST00000680941.1:c.*248+47C>T	ENSP00000506378.1:n.*248+47C>T
ENST00000311852.10:c.850+47C>T	ENSP00000308208.6:n.850+47C>T
ENST00000548162.1:n.1092+47C>T
NM_004995.3:c.850+47C>T	NP_004986.1:n.850+47C>T
NM_004995.4:c.850+47C>T MANE Select	NP_004986.1:n.850+47C>T