Canonical Allele Identifier: CA1943151997

Gene: ADAM12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126093840C= , CM000672.2:g.126093840C=	GRCh38
NC_000010.10:g.127782409C= , CM000672.1:g.127782409C=	GRCh37
NC_000010.9:g.127772399C=	NCBI36
NG_029050.1:g.299719G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001288973.2:c.1145+145G= MANE Select	NP_001275902.1:n.1145+145G=
ENST00000448723.2:c.1145+145G= MANE Select	ENSP00000391268.2:n.1145+145G=
NM_001288973.1:c.1145+145G=	NP_001275902.1:n.1145+145G=
NM_001288974.1:c.1145+145G=	NP_001275903.1:n.1145+145G=
NM_001288974.2:c.1145+145G=	NP_001275903.1:n.1145+145G=
NM_001288975.1:c.1145+145G=	NP_001275904.1:n.1145+145G=
NM_001288975.2:c.1145+145G=	NP_001275904.1:n.1145+145G=
NM_003474.5:c.1154+145G=	NP_003465.3:n.1154+145G=
NM_003474.6:c.1154+145G=	NP_003465.3:n.1154+145G=
NM_021641.4:c.1154+145G=	NP_067673.2:n.1154+145G=
NM_021641.5:c.1154+145G=	NP_067673.2:n.1154+145G=
ENST00000368676.8:c.1154+145G=	ENSP00000357665.4:n.1154+145G=
ENST00000368679.8:c.1154+145G=	ENSP00000357668.4:n.1154+145G=
ENST00000485388.2:n.124-2847G=
XM_017016705.1:c.686+145G=	XP_016872194.1:n.686+145G=