Canonical Allele Identifier: CA1943159722

Gene: ADAM12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126134582T= , CM000672.2:g.126134582T=	GRCh38
NC_000010.10:g.127823151T= , CM000672.1:g.127823151T=	GRCh37
NC_000010.9:g.127813141T=	NCBI36
NG_029050.1:g.258977A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001288973.2:c.416+1002A= MANE Select	NP_001275902.1:n.416+1002A=
ENST00000448723.2:c.416+1002A= MANE Select	ENSP00000391268.2:n.416+1002A=
NM_001288973.1:c.416+1002A=	NP_001275902.1:n.416+1002A=
NM_001288974.1:c.416+1002A=	NP_001275903.1:n.416+1002A=
NM_001288974.2:c.416+1002A=	NP_001275903.1:n.416+1002A=
NM_001288975.1:c.416+1002A=	NP_001275904.1:n.416+1002A=
NM_001288975.2:c.416+1002A=	NP_001275904.1:n.416+1002A=
NM_003474.5:c.425+1002A=	NP_003465.3:n.425+1002A=
NM_003474.6:c.425+1002A=	NP_003465.3:n.425+1002A=
NM_021641.4:c.425+1002A=	NP_067673.2:n.425+1002A=
NM_021641.5:c.425+1002A=	NP_067673.2:n.425+1002A=
ENST00000368676.8:c.425+1002A=	ENSP00000357665.4:n.425+1002A=
ENST00000368679.8:c.425+1002A=	ENSP00000357668.4:n.425+1002A=
ENST00000448723.1:c.416+1002A=	ENSP00000391268.1:n.416+1002A=
XM_017016705.1:c.-44+1002A=	XP_016872194.1:n.-44+1002A=