Canonical Allele Identifier: CA661273621

Gene: ADAM12

Linked Data

• dbSNP Id: rs1176138347
• gnomAD v3: 10-126140414-A-G
• gnomAD v4: 10-126140414-A-G
• MyVariant Identifiers: chr10:g.127828983A>G (hg19) ; chr10:g.126140414A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126140414A>G , CM000672.2:g.126140414A>G	GRCh38
NC_000010.10:g.127828983A>G , CM000672.1:g.127828983A>G	GRCh37
NC_000010.9:g.127818973A>G	NCBI36
NG_029050.1:g.253145T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448723.2:c.340-4754T>C MANE Select	ENSP00000391268.2:n.340-4754T>C
ENST00000368676.8:c.349-4754T>C	ENSP00000357665.4:n.349-4754T>C
ENST00000368679.8:c.349-4754T>C	ENSP00000357668.4:n.349-4754T>C
ENST00000448723.1:c.340-4754T>C	ENSP00000391268.1:n.340-4754T>C
ENST00000494661.1:n.80-4754T>C
NM_001288973.1:c.340-4754T>C	NP_001275902.1:n.340-4754T>C
NM_001288974.1:c.340-4754T>C	NP_001275903.1:n.340-4754T>C
NM_001288975.1:c.340-4754T>C	NP_001275904.1:n.340-4754T>C
NM_003474.5:c.349-4754T>C	NP_003465.3:n.349-4754T>C
NM_021641.4:c.349-4754T>C	NP_067673.2:n.349-4754T>C
XM_017016705.1:c.-120-4754T>C	XP_016872194.1:n.-120-4754T>C
NM_001288973.2:c.340-4754T>C MANE Select	NP_001275902.1:n.340-4754T>C
NM_001288974.2:c.340-4754T>C	NP_001275903.1:n.340-4754T>C
NM_001288975.2:c.340-4754T>C	NP_001275904.1:n.340-4754T>C
NM_003474.6:c.349-4754T>C	NP_003465.3:n.349-4754T>C
NM_021641.5:c.349-4754T>C	NP_067673.2:n.349-4754T>C