Canonical Allele Identifier: CA2123185307
Gene: MMP14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843319A= , CM000676.2:g.22843319A= GRCh38
NC_000014.8:g.23312528A= , CM000676.1:g.23312528A= GRCh37
NC_000014.7:g.22382368A= NCBI36
NG_046989.1:g.11787A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.751A= MANE Select ENSP00000308208.6:p.Ser251=
ENST00000548162.2:c.751A= ENSP00000506068.1:p.Ser251=
ENST00000680097.1:c.*66A= ENSP00000506631.1:n.*66A=
ENST00000680941.1:c.*149A= ENSP00000506378.1:n.*149A=
ENST00000311852.10:c.751A= ENSP00000308208.6:p.Ser251=
ENST00000548162.1:n.993A=
NM_004995.3:c.751A= NP_004986.1:p.Ser251=
NM_004995.4:c.751A= MANE Select NP_004986.1:p.Ser251=