Canonical Allele Identifier: CA2361573555

Gene: MMP24 MMP24OS

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35261344G= , CM000682.2:g.35261344G=	GRCh38
NC_000020.10:g.33849147G= , CM000682.1:g.33849147G=	GRCh37
NC_000020.9:g.33312563G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000246186.8:c.818-2447G= (MMP24) MANE Select	ENSP00000246186.6:n.818-2447G=
ENST00000246186.7:c.818-2447G= (MMP24)	ENSP00000246186.6:n.818-2447G=
ENST00000433764.5:n.221+10661C= (MMP24OS)
ENST00000438751.5:n.237+10661C= (MMP24OS)
ENST00000453892.1:n.53-4938C= (MMP24OS)
ENST00000454184.5:n.227+10661C= (MMP24OS)
ENST00000456350.5:n.236+10661C= (MMP24OS)
ENST00000566203.6:n.255+10661C= (MMP24OS)
ENST00000635104.1:n.197+10661C= (MMP24OS)
NM_006690.3:c.818-2447G= (MMP24)	NP_006681.1:n.818-2447G=
XM_011528500.1:c.818-2447G= (MMP24)	XP_011526802.1:n.818-2447G=
NM_001355008.1:c.-463+10661C=	NP_001341937.1:n.-463+10661C=
XM_011528500.2:c.818-2447G= (MMP24)	XP_011526802.1:n.818-2447G=
XM_017027597.1:c.818-5861G= (MMP24)	XP_016883086.1:n.818-5861G=
XM_017027598.1:c.725-2447G= (MMP24)	XP_016883087.1:n.725-2447G=
NM_006690.4:c.818-2447G= (MMP24) MANE Select	NP_006681.1:n.818-2447G=
NM_001355008.2:c.-463+10661C=	NP_001341937.1:n.-463+10661C=