Canonical Allele Identifier: CA1800558107

Gene: MMP16

Linked Data

• dbSNP Id: rs1824717

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88063751T>A , CM000670.2:g.88063751T>A	GRCh38
NC_000008.10:g.89075979T>A , CM000670.1:g.89075979T>A	GRCh37
NC_000008.9:g.89145095T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000286614.11:c.1223-7473A>T MANE Select	ENSP00000286614.6:n.1223-7473A>T
ENST00000286614.10:c.1223-7473A>T	ENSP00000286614.6:n.1223-7473A>T
NM_005941.4:c.1223-7473A>T	NP_005932.2:n.1223-7473A>T
XM_011517039.1:c.1223-7473A>T	XP_011515341.1:n.1223-7473A>T
XM_011517040.1:c.1223-7473A>T	XP_011515342.1:n.1223-7473A>T
XM_011517041.1:c.1094-7473A>T	XP_011515343.1:n.1094-7473A>T
XR_928334.1:n.1505-7473A>T
XM_024447154.1:c.434-7473A>T	XP_024302922.1:n.434-7473A>T
NM_005941.5:c.1223-7473A>T MANE Select	NP_005932.2:n.1223-7473A>T