Canonical Allele Identifier: CA378686400

Gene: ADAM12

Linked Data

• dbSNP Id: rs1278279
• MyVariant Identifiers: chr10:g.127753478G>C (hg19) ; chr10:g.126064909G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126064909G>C , CM000672.2:g.126064909G>C	GRCh38
NC_000010.10:g.127753478G>C , CM000672.1:g.127753478G>C	GRCh37
NC_000010.9:g.127743468G>C	NCBI36
NG_029050.1:g.328650C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000448723.2:c.1506C>G MANE Select	ENSP00000391268.2:p.Asn502Lys
ENST00000368676.8:c.1515C>G	ENSP00000357665.4:p.Asn505Lys
ENST00000368679.8:c.1515C>G	ENSP00000357668.4:p.Asn505Lys
ENST00000467145.1:n.430C>G
ENST00000482291.1:n.383C>G
NM_001288973.1:c.1506C>G	NP_001275902.1:p.Asn502Lys
NM_001288974.1:c.1506C>G	NP_001275903.1:p.Asn502Lys
NM_001288975.1:c.1506C>G	NP_001275904.1:p.Asn502Lys
NM_003474.5:c.1515C>G	NP_003465.3:p.Asn505Lys
NM_021641.4:c.1515C>G	NP_067673.2:p.Asn505Lys
XM_017016705.1:c.1047C>G	XP_016872194.1:p.Asn349Lys
XM_017016706.1:c.348C>G	XP_016872195.1:p.Asn116Lys
XM_024448210.1:c.177C>G	XP_024303978.1:p.Asn59Lys
NM_001288973.2:c.1506C>G MANE Select	NP_001275902.1:p.Asn502Lys
NM_001288974.2:c.1506C>G	NP_001275903.1:p.Asn502Lys
NM_001288975.2:c.1506C>G	NP_001275904.1:p.Asn502Lys
NM_003474.6:c.1515C>G	NP_003465.3:p.Asn505Lys
NM_021641.5:c.1515C>G	NP_067673.2:p.Asn505Lys