Canonical Allele Identifier: CA382216362

Gene: MMP27

Linked Data

• MyVariant Identifiers: chr11:g.102567110A>T (hg19) ; chr11:g.102696379A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.102696379A>T , CM000673.2:g.102696379A>T	GRCh38
NC_000011.9:g.102567110A>T , CM000673.1:g.102567110A>T	GRCh37
NC_000011.8:g.102072320A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260229.5:c.894T>A MANE Select	ENSP00000260229.4:p.Phe298Leu
ENST00000260229.4:c.894T>A	ENSP00000260229.4:p.Phe298Leu
NM_022122.2:c.894T>A	NP_071405.2:p.Phe298Leu
XM_011542948.1:c.765T>A	XP_011541250.1:p.Phe255Leu
XM_011542949.1:c.732T>A	XP_011541251.1:p.Phe244Leu
XM_011542950.1:c.579T>A	XP_011541252.1:p.Phe193Leu
XM_011542951.1:c.894T>A	XP_011541253.1:p.Phe298Leu
XM_011542948.2:c.765T>A	XP_011541250.1:p.Phe255Leu
XM_011542949.2:c.732T>A	XP_011541251.1:p.Phe244Leu
XM_011542950.3:c.579T>A	XP_011541252.1:p.Phe193Leu
XM_017018120.1:c.891T>A	XP_016873609.1:p.Phe297Leu
NM_022122.3:c.894T>A MANE Select	NP_071405.2:p.Phe298Leu