Canonical Allele Identifier: CA1943162313

Gene: ADAM12

Linked Data

• dbSNP Id: rs1590484310

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126140490A>C , CM000672.2:g.126140490A>C	GRCh38
NC_000010.10:g.127829059A>C , CM000672.1:g.127829059A>C	GRCh37
NC_000010.9:g.127819049A>C	NCBI36
NG_029050.1:g.253069T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000448723.2:c.340-4830T>G MANE Select	ENSP00000391268.2:n.340-4830T>G
ENST00000368676.8:c.349-4830T>G	ENSP00000357665.4:n.349-4830T>G
ENST00000368679.8:c.349-4830T>G	ENSP00000357668.4:n.349-4830T>G
ENST00000448723.1:c.340-4830T>G	ENSP00000391268.1:n.340-4830T>G
ENST00000494661.1:n.80-4830T>G
NM_001288973.1:c.340-4830T>G	NP_001275902.1:n.340-4830T>G
NM_001288974.1:c.340-4830T>G	NP_001275903.1:n.340-4830T>G
NM_001288975.1:c.340-4830T>G	NP_001275904.1:n.340-4830T>G
NM_003474.5:c.349-4830T>G	NP_003465.3:n.349-4830T>G
NM_021641.4:c.349-4830T>G	NP_067673.2:n.349-4830T>G
XM_017016705.1:c.-120-4830T>G	XP_016872194.1:n.-120-4830T>G
NM_001288973.2:c.340-4830T>G MANE Select	NP_001275902.1:n.340-4830T>G
NM_001288974.2:c.340-4830T>G	NP_001275903.1:n.340-4830T>G
NM_001288975.2:c.340-4830T>G	NP_001275904.1:n.340-4830T>G
NM_003474.6:c.349-4830T>G	NP_003465.3:n.349-4830T>G
NM_021641.5:c.349-4830T>G	NP_067673.2:n.349-4830T>G