Canonical Allele Identifier: CA2123185332

Gene: MMP14

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22843393C= , CM000676.2:g.22843393C=	GRCh38
NC_000014.8:g.23312602C= , CM000676.1:g.23312602C=	GRCh37
NC_000014.7:g.22382442C=	NCBI36
NG_046989.1:g.11861C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311852.11:c.825C= MANE Select	ENSP00000308208.6:p.Asp275=
ENST00000548162.2:c.825C=	ENSP00000506068.1:p.Asp275=
ENST00000680097.1:c.*140C=	ENSP00000506631.1:n.*140C=
ENST00000680941.1:c.*223C=	ENSP00000506378.1:n.*223C=
ENST00000311852.10:c.825C=	ENSP00000308208.6:p.Asp275=
ENST00000548162.1:n.1067C=
NM_004995.3:c.825C=	NP_004986.1:p.Asp275=
NM_004995.4:c.825C= MANE Select	NP_004986.1:p.Asp275=