Canonical Allele Identifier: CA6881918

Gene: MMP17

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131844051C>T , CM000674.2:g.131844051C>T	GRCh38
NC_000012.11:g.132328596C>T , CM000674.1:g.132328596C>T	GRCh37
NC_000012.10:g.130894549C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000535004.2:c.938C>T	ENSP00000445620.2:p.Pro313Leu
ENST00000545790.6:c.938C>T	ENSP00000441710.2:p.Pro313Leu
ENST00000360564.5:c.938C>T MANE Select	ENSP00000353767.1:p.Pro313Leu
ENST00000534865.1:c.461C>T	ENSP00000442104.1:p.Pro154Leu
ENST00000535182.1:n.353C>T
ENST00000535291.5:c.686C>T	ENSP00000441106.1:p.Pro229Leu
ENST00000542142.1:n.88C>T
NM_016155.4:c.938C>T	NP_057239.4:p.Pro313Leu
XM_011538355.1:c.686C>T	XP_011536657.1:p.Pro229Leu
XM_011538356.1:c.686C>T	XP_011536658.1:p.Pro229Leu
XM_011538357.1:c.686C>T	XP_011536659.1:p.Pro229Leu
XR_944550.1:n.1026C>T
XR_944551.1:n.1026C>T
XR_944552.1:n.1026C>T
NM_016155.6:c.938C>T	NP_057239.4:p.Pro313Leu
XM_011538355.3:c.686C>T	XP_011536657.1:p.Pro229Leu
XM_011538356.3:c.686C>T	XP_011536658.1:p.Pro229Leu
XM_011538357.2:c.686C>T	XP_011536659.1:p.Pro229Leu
XM_017019307.1:c.938C>T	XP_016874796.1:p.Pro313Leu
XR_001748705.1:n.1019C>T
XR_944550.2:n.1019C>T
XR_944551.2:n.1019C>T
XR_944552.2:n.1019C>T
NM_016155.7:c.938C>T MANE Select	NP_057239.4:p.Pro313Leu