Canonical Allele Identifier: CA485591261

Gene: MMP14

Linked Data

• MyVariant Identifiers: chr14:g.23312560C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.22843351C>T , CM000676.2:g.22843351C>T	GRCh38
NC_000014.8:g.23312560C>T , CM000676.1:g.23312560C>T	GRCh37
NC_000014.7:g.22382400C>T	NCBI36
NG_046989.1:g.11819C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311852.11:c.783C>T MANE Select	ENSP00000308208.6:p.Tyr261=
ENST00000548162.2:c.783C>T	ENSP00000506068.1:p.Tyr261=
ENST00000680097.1:c.*98C>T	ENSP00000506631.1:n.*98C>T
ENST00000680941.1:c.*181C>T	ENSP00000506378.1:n.*181C>T
ENST00000311852.10:c.783C>T	ENSP00000308208.6:p.Tyr261=
ENST00000548162.1:n.1025C>T
NM_004995.3:c.783C>T	NP_004986.1:p.Tyr261=
NM_004995.4:c.783C>T MANE Select	NP_004986.1:p.Tyr261=