Canonical Allele Identifier: CA12793851

Gene: MMP16

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88195036C>A , CM000670.2:g.88195036C>A	GRCh38
NC_000008.10:g.89207265C>A , CM000670.1:g.89207265C>A	GRCh37
NC_000008.9:g.89276381C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286614.11:c.281+2122G>T MANE Select	ENSP00000286614.6:n.281+2122G>T
ENST00000286614.10:c.281+2122G>T	ENSP00000286614.6:n.281+2122G>T
ENST00000520568.1:n.331+2122G>T
ENST00000522726.1:c.332+2122G>T	ENSP00000429147.1:n.332+2122G>T
ENST00000544227.5:n.281+2122G>T
NM_005941.4:c.281+2122G>T	NP_005932.2:n.281+2122G>T
XM_011517039.1:c.281+2122G>T	XP_011515341.1:n.281+2122G>T
XM_011517040.1:c.281+2122G>T	XP_011515342.1:n.281+2122G>T
XM_011517041.1:c.152+2122G>T	XP_011515343.1:n.152+2122G>T
XM_011517042.1:c.281+2122G>T	XP_011515344.1:n.281+2122G>T
XR_928334.1:n.563+2122G>T
NM_005941.5:c.281+2122G>T MANE Select	NP_005932.2:n.281+2122G>T