Canonical Allele Identifier: CA1800629763

Gene: MMP16

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88259833G= , CM000670.2:g.88259833G=	GRCh38
NC_000008.10:g.89272062G= , CM000670.1:g.89272062G=	GRCh37
NC_000008.9:g.89341178G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286614.11:c.133-62527C= MANE Select	ENSP00000286614.6:n.133-62527C=
ENST00000286614.10:c.133-62527C=	ENSP00000286614.6:n.133-62527C=
ENST00000520568.1:n.183-62527C=
ENST00000522726.1:c.184-62527C=	ENSP00000429147.1:n.184-62527C=
ENST00000544227.5:n.133-62527C=
NM_005941.4:c.133-62527C=	NP_005932.2:n.133-62527C=
XM_011517039.1:c.133-62527C=	XP_011515341.1:n.133-62527C=
XM_011517040.1:c.133-62527C=	XP_011515342.1:n.133-62527C=
XM_011517042.1:c.133-62527C=	XP_011515344.1:n.133-62527C=
XR_928334.1:n.415-62527C=
NM_005941.5:c.133-62527C= MANE Select	NP_005932.2:n.133-62527C=