Canonical Allele Identifier: CA117271073

Gene: ADAMTS12

Linked Data

• dbSNP Id: rs896764249
• gnomAD v2: 5-33879787-A-G
• gnomAD v3: 5-33879682-A-G
• gnomAD v4: 5-33879682-A-G
• MyVariant Identifiers: chr5:g.33879787A>G (hg19) ; chr5:g.33879682A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33879682A>G , CM000667.2:g.33879682A>G	GRCh38
NC_000005.9:g.33879787A>G , CM000667.1:g.33879787A>G	GRCh37
NC_000005.8:g.33915544A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504830.6:c.489+1437T>C MANE Select	ENSP00000422554.1:n.489+1437T>C
ENST00000352040.7:c.489+1437T>C	ENSP00000344847.3:n.489+1437T>C
ENST00000504830.5:c.489+1437T>C	ENSP00000422554.1:n.489+1437T>C
ENST00000515401.1:c.489+1437T>C	ENSP00000421638.1:n.489+1437T>C
NM_030955.2:c.489+1437T>C	NP_112217.2:n.489+1437T>C
XM_011514146.1:c.489+1437T>C	XP_011512448.1:n.489+1437T>C
XM_011514148.1:c.489+1437T>C	XP_011512450.1:n.489+1437T>C
XM_011514149.1:c.489+1437T>C	XP_011512451.1:n.489+1437T>C
NM_001324511.1:c.489+1437T>C	NP_001311440.1:n.489+1437T>C
NM_001324512.1:c.489+1437T>C	NP_001311441.1:n.489+1437T>C
NM_030955.3:c.489+1437T>C	NP_112217.2:n.489+1437T>C
XM_017009905.1:c.489+1437T>C	XP_016865394.1:n.489+1437T>C
NM_030955.4:c.489+1437T>C MANE Select	NP_112217.2:n.489+1437T>C
NM_001324511.2:c.489+1437T>C	NP_001311440.1:n.489+1437T>C
NM_001324512.2:c.489+1437T>C	NP_001311441.1:n.489+1437T>C