Canonical Allele Identifier: CA2123185302
Gene: MMP14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.22843301C= , CM000676.2:g.22843301C= GRCh38
NC_000014.8:g.23312510C= , CM000676.1:g.23312510C= GRCh37
NC_000014.7:g.22382350C= NCBI36
NG_046989.1:g.11769C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311852.11:c.733C= MANE Select ENSP00000308208.6:p.Leu245=
ENST00000548162.2:c.733C= ENSP00000506068.1:p.Leu245=
ENST00000680097.1:c.*48C= ENSP00000506631.1:n.*48C=
ENST00000680941.1:c.*131C= ENSP00000506378.1:n.*131C=
ENST00000311852.10:c.733C= ENSP00000308208.6:p.Leu245=
ENST00000548162.1:n.975C=
NM_004995.3:c.733C= NP_004986.1:p.Leu245=
NM_004995.4:c.733C= MANE Select NP_004986.1:p.Leu245=