Canonical Allele Identifier: CA6881618

Gene: MMP17

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131838311G>C , CM000674.2:g.131838311G>C	GRCh38
NC_000012.11:g.132322856G>C , CM000674.1:g.132322856G>C	GRCh37
NC_000012.10:g.130888809G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000535004.2:c.276G>C	ENSP00000445620.2:p.Glu92Asp
ENST00000545671.6:c.160-301G>C	ENSP00000444603.2:n.160-301G>C
ENST00000545790.6:c.276G>C	ENSP00000441710.2:p.Glu92Asp
ENST00000360564.5:c.276G>C MANE Select	ENSP00000353767.1:p.Glu92Asp
ENST00000535291.5:c.24G>C	ENSP00000441106.1:p.Glu8Asp
ENST00000545671.5:c.-20-301G>C	ENSP00000444603.1:n.-20-301G>C
ENST00000545790.5:c.24G>C	ENSP00000441710.1:p.Glu8Asp
NM_016155.4:c.276G>C	NP_057239.4:p.Glu92Asp
XM_011538355.1:c.24G>C	XP_011536657.1:p.Glu8Asp
XM_011538356.1:c.24G>C	XP_011536658.1:p.Glu8Asp
XM_011538357.1:c.24G>C	XP_011536659.1:p.Glu8Asp
XR_944550.1:n.364G>C
XR_944551.1:n.364G>C
XR_944552.1:n.364G>C
NM_016155.6:c.276G>C	NP_057239.4:p.Glu92Asp
XM_011538355.3:c.24G>C	XP_011536657.1:p.Glu8Asp
XM_011538356.3:c.24G>C	XP_011536658.1:p.Glu8Asp
XM_011538357.2:c.24G>C	XP_011536659.1:p.Glu8Asp
XM_017019307.1:c.276G>C	XP_016874796.1:p.Glu92Asp
XR_001748705.1:n.357G>C
XR_944550.2:n.357G>C
XR_944551.2:n.357G>C
XR_944552.2:n.357G>C
NM_016155.7:c.276G>C MANE Select	NP_057239.4:p.Glu92Asp