Canonical Allele Identifier: CA1943162292

Gene: ADAM12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126140445_126140446delinsTG , CM000672.2:g.126140445_126140446delinsTG	GRCh38
NC_000010.10:g.127829014_127829015delinsTG , CM000672.1:g.127829014_127829015delinsTG	GRCh37
NC_000010.9:g.127819004_127819005delinsTG	NCBI36
NG_029050.1:g.253113_253114delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448723.2:c.340-4786_340-4785delinsCA MANE Select	ENSP00000391268.2:n.340-4786_340-4785delinsCA
ENST00000368676.8:c.349-4786_349-4785delinsCA	ENSP00000357665.4:n.349-4786_349-4785delinsCA
ENST00000368679.8:c.349-4786_349-4785delinsCA	ENSP00000357668.4:n.349-4786_349-4785delinsCA
ENST00000448723.1:c.340-4786_340-4785delinsCA	ENSP00000391268.1:n.340-4786_340-4785delinsCA
ENST00000494661.1:n.80-4786_80-4785delinsCA
NM_001288973.1:c.340-4786_340-4785delinsCA	NP_001275902.1:n.340-4786_340-4785delinsCA
NM_001288974.1:c.340-4786_340-4785delinsCA	NP_001275903.1:n.340-4786_340-4785delinsCA
NM_001288975.1:c.340-4786_340-4785delinsCA	NP_001275904.1:n.340-4786_340-4785delinsCA
NM_003474.5:c.349-4786_349-4785delinsCA	NP_003465.3:n.349-4786_349-4785delinsCA
NM_021641.4:c.349-4786_349-4785delinsCA	NP_067673.2:n.349-4786_349-4785delinsCA
XM_017016705.1:c.-120-4786_-120-4785delinsCA	XP_016872194.1:n.-120-4786_-120-4785delinsCA
NM_001288973.2:c.340-4786_340-4785delinsCA MANE Select	NP_001275902.1:n.340-4786_340-4785delinsCA
NM_001288974.2:c.340-4786_340-4785delinsCA	NP_001275903.1:n.340-4786_340-4785delinsCA
NM_001288975.2:c.340-4786_340-4785delinsCA	NP_001275904.1:n.340-4786_340-4785delinsCA
NM_003474.6:c.349-4786_349-4785delinsCA	NP_003465.3:n.349-4786_349-4785delinsCA
NM_021641.5:c.349-4786_349-4785delinsCA	NP_067673.2:n.349-4786_349-4785delinsCA