Canonical Allele Identifier: CA5741013

Gene: ADAM12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126330456C>G , CM000672.2:g.126330456C>G	GRCh38
NC_000010.10:g.128019025C>G , CM000672.1:g.128019025C>G	GRCh37
NC_000010.9:g.128009015C>G	NCBI36
NG_029050.1:g.63103G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001288973.2:c.142G>C MANE Select	NP_001275902.1:p.Gly48Arg
ENST00000448723.2:c.142G>C MANE Select	ENSP00000391268.2:p.Gly48Arg
NM_001288973.1:c.142G>C	NP_001275902.1:p.Gly48Arg
NM_001288974.1:c.142G>C	NP_001275903.1:p.Gly48Arg
NM_001288974.2:c.142G>C	NP_001275903.1:p.Gly48Arg
NM_001288975.1:c.142G>C	NP_001275904.1:p.Gly48Arg
NM_001288975.2:c.142G>C	NP_001275904.1:p.Gly48Arg
NM_003474.5:c.142G>C	NP_003465.3:p.Gly48Arg
NM_003474.6:c.142G>C	NP_003465.3:p.Gly48Arg
NM_021641.4:c.142G>C	NP_067673.2:p.Gly48Arg
NM_021641.5:c.142G>C	NP_067673.2:p.Gly48Arg
ENST00000368676.8:c.142G>C	ENSP00000357665.4:p.Gly48Arg
ENST00000368679.8:c.142G>C	ENSP00000357668.4:p.Gly48Arg
ENST00000448723.1:c.142G>C	ENSP00000391268.1:p.Gly48Arg