Canonical Allele Identifier: CA2361573537

Gene: MMP24 MMP24OS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35261289T= , CM000682.2:g.35261289T=	GRCh38
NC_000020.10:g.33849092T= , CM000682.1:g.33849092T=	GRCh37
NC_000020.9:g.33312508T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000246186.8:c.818-2502T= (MMP24) MANE Select	ENSP00000246186.6:n.818-2502T=
ENST00000246186.7:c.818-2502T= (MMP24)	ENSP00000246186.6:n.818-2502T=
ENST00000433764.5:n.221+10716A= (MMP24OS)
ENST00000438751.5:n.237+10716A= (MMP24OS)
ENST00000453892.1:n.53-4883A= (MMP24OS)
ENST00000454184.5:n.227+10716A= (MMP24OS)
ENST00000456350.5:n.236+10716A= (MMP24OS)
ENST00000566203.6:n.255+10716A= (MMP24OS)
ENST00000635104.1:n.197+10716A= (MMP24OS)
NM_006690.3:c.818-2502T= (MMP24)	NP_006681.1:n.818-2502T=
XM_011528500.1:c.818-2502T= (MMP24)	XP_011526802.1:n.818-2502T=
NM_001355008.1:c.-463+10716A=	NP_001341937.1:n.-463+10716A=
XM_011528500.2:c.818-2502T= (MMP24)	XP_011526802.1:n.818-2502T=
XM_017027597.1:c.818-5916T= (MMP24)	XP_016883086.1:n.818-5916T=
XM_017027598.1:c.725-2502T= (MMP24)	XP_016883087.1:n.725-2502T=
NM_006690.4:c.818-2502T= (MMP24) MANE Select	NP_006681.1:n.818-2502T=
NM_001355008.2:c.-463+10716A=	NP_001341937.1:n.-463+10716A=