Canonical Allele Identifier: CA1800611504

Gene: MMP16

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88192609T= , CM000670.2:g.88192609T=	GRCh38
NC_000008.10:g.89204838T= , CM000670.1:g.89204838T=	GRCh37
NC_000008.9:g.89273954T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286614.11:c.281+4549A= MANE Select	ENSP00000286614.6:n.281+4549A=
ENST00000286614.10:c.281+4549A=	ENSP00000286614.6:n.281+4549A=
ENST00000520568.1:n.331+4549A=
ENST00000522726.1:c.332+4549A=	ENSP00000429147.1:n.332+4549A=
ENST00000544227.5:n.281+4549A=
NM_005941.4:c.281+4549A=	NP_005932.2:n.281+4549A=
XM_011517039.1:c.281+4549A=	XP_011515341.1:n.281+4549A=
XM_011517040.1:c.281+4549A=	XP_011515342.1:n.281+4549A=
XM_011517041.1:c.152+4549A=	XP_011515343.1:n.152+4549A=
XM_011517042.1:c.281+4549A=	XP_011515344.1:n.281+4549A=
XR_928334.1:n.563+4549A=
NM_005941.5:c.281+4549A= MANE Select	NP_005932.2:n.281+4549A=