Canonical Allele Identifier: CA1800574635

Gene: MMP16

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88107455C= , CM000670.2:g.88107455C=	GRCh38
NC_000008.10:g.89119683C= , CM000670.1:g.89119683C=	GRCh37
NC_000008.9:g.89188799C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005941.5:c.1083+9052G= MANE Select	NP_005932.2:n.1083+9052G=
ENST00000286614.11:c.1083+9052G= MANE Select	ENSP00000286614.6:n.1083+9052G=
NM_005941.4:c.1083+9052G=	NP_005932.2:n.1083+9052G=
ENST00000286614.10:c.1083+9052G=	ENSP00000286614.6:n.1083+9052G=
ENST00000544227.5:n.1083+9052G=
XM_011517039.1:c.1083+9052G=	XP_011515341.1:n.1083+9052G=
XM_011517040.1:c.1083+9052G=	XP_011515342.1:n.1083+9052G=
XM_011517041.1:c.954+9052G=	XP_011515343.1:n.954+9052G=
XM_011517042.1:c.1083+9052G=	XP_011515344.1:n.1083+9052G=
XM_024447154.1:c.294+9052G=	XP_024302922.1:n.294+9052G=
XR_928334.1:n.1365+9052G=