Canonical Allele Identifier: CA635342162

Gene: MMP24 MMP24OS

Linked Data

• gnomAD v2: 20-33849029-CCAGGGGAGTTGGCTTTCAGAGGATCTGGTTGCTGGCGCTCCACTGGCCTCGTGCTTCCTTTCTGGT-C
• gnomAD v3: 20-35261226-CCAGGGGAGTTGGCTTTCAGAGGATCTGGTTGCTGGCGCTCCACTGGCCTCGTGCTTCCTTTCTGGT-C
• gnomAD v4: 20-35261226-CCAGGGGAGTTGGCTTTCAGAGGATCTGGTTGCTGGCGCTCCACTGGCCTCGTGCTTCCTTTCTGGT-C
• MyVariant Identifiers: chr20:g.33849030_33849095del (hg19) ; chr20:g.35261227_35261292del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.35261229_35261294del , CM000682.2:g.35261229_35261294del	GRCh38
NC_000020.10:g.33849032_33849097del , CM000682.1:g.33849032_33849097del	GRCh37
NC_000020.9:g.33312448_33312513del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000246186.8:c.818-2562_818-2497del (MMP24) MANE Select	ENSP00000246186.6:n.818-2562_818-2497del
ENST00000246186.7:c.818-2562_818-2497del (MMP24)	ENSP00000246186.6:n.818-2562_818-2497del
ENST00000433764.5:n.221+10713_221+10778del (MMP24OS)
ENST00000438751.5:n.237+10713_237+10778del (MMP24OS)
ENST00000453892.1:n.53-4886_53-4821del (MMP24OS)
ENST00000454184.5:n.227+10713_227+10778del (MMP24OS)
ENST00000456350.5:n.236+10713_236+10778del (MMP24OS)
ENST00000566203.6:n.255+10713_255+10778del (MMP24OS)
ENST00000635104.1:n.197+10713_197+10778del (MMP24OS)
NM_006690.3:c.818-2562_818-2497del (MMP24)	NP_006681.1:n.818-2562_818-2497del
XM_011528500.1:c.818-2562_818-2497del (MMP24)	XP_011526802.1:n.818-2562_818-2497del
NM_001355008.1:c.-463+10713_-463+10778del	NP_001341937.1:n.-463+10713_-463+10778del...
XM_011528500.2:c.818-2562_818-2497del (MMP24)	XP_011526802.1:n.818-2562_818-2497del
XM_017027597.1:c.818-5976_818-5911del (MMP24)	XP_016883086.1:n.818-5976_818-5911del
XM_017027598.1:c.725-2562_725-2497del (MMP24)	XP_016883087.1:n.725-2562_725-2497del
NM_006690.4:c.818-2562_818-2497del (MMP24) MANE Select	NP_006681.1:n.818-2562_818-2497del
NM_001355008.2:c.-463+10713_-463+10778del	NP_001341937.1:n.-463+10713_-463+10778del...