Canonical Allele Identifier: CA2123185299

Gene: MMP14

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22843297T= , CM000676.2:g.22843297T=	GRCh38
NC_000014.8:g.23312506T= , CM000676.1:g.23312506T=	GRCh37
NC_000014.7:g.22382346T=	NCBI36
NG_046989.1:g.11765T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311852.11:c.729T= MANE Select	ENSP00000308208.6:p.His243=
ENST00000548162.2:c.729T=	ENSP00000506068.1:p.His243=
ENST00000680097.1:c.*44T=	ENSP00000506631.1:n.*44T=
ENST00000680941.1:c.*127T=	ENSP00000506378.1:n.*127T=
ENST00000311852.10:c.729T=	ENSP00000308208.6:p.His243=
ENST00000548162.1:n.971T=
NM_004995.3:c.729T=	NP_004986.1:p.His243=
NM_004995.4:c.729T= MANE Select	NP_004986.1:p.His243=