Canonical Allele Identifier: CA387282647

Gene: MMP17

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.131828519C>G , CM000674.2:g.131828519C>G	GRCh38
NC_000012.11:g.132313064C>G , CM000674.1:g.132313064C>G	GRCh37
NC_000012.10:g.130879017C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000535004.2:c.25C>G	ENSP00000445620.2:p.Pro9Ala
ENST00000545671.6:c.25C>G	ENSP00000444603.2:p.Pro9Ala
ENST00000545790.6:c.25C>G	ENSP00000441710.2:p.Pro9Ala
ENST00000360564.5:c.25C>G MANE Select	ENSP00000353767.1:p.Pro9Ala
ENST00000545671.5:c.-155C>G	ENSP00000444603.1:n.-155C>G
NM_016155.4:c.25C>G	NP_057239.4:p.Pro9Ala
XR_944550.1:n.113C>G
XR_944551.1:n.113C>G
XR_944552.1:n.113C>G
NM_016155.6:c.25C>G	NP_057239.4:p.Pro9Ala
XM_017019307.1:c.25C>G	XP_016874796.1:p.Pro9Ala
XR_001748705.1:n.106C>G
XR_944550.2:n.106C>G
XR_944551.2:n.106C>G
XR_944552.2:n.106C>G
NM_016155.7:c.25C>G MANE Select	NP_057239.4:p.Pro9Ala