Canonical Allele Identifier: CA2549194721
Gene: ADAM12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.126140474del , CM000672.2:g.126140474del GRCh38
NC_000010.10:g.127829043del , CM000672.1:g.127829043del GRCh37
NC_000010.9:g.127819033del NCBI36
NG_029050.1:g.253090del

Transcript Alleles

HGVS Amino-acid change
ENST00000448723.2:c.340-4809del MANE Select ENSP00000391268.2:n.340-4809del
ENST00000368676.8:c.349-4809del ENSP00000357665.4:n.349-4809del
ENST00000368679.8:c.349-4809del ENSP00000357668.4:n.349-4809del
ENST00000448723.1:c.340-4809del ENSP00000391268.1:n.340-4809del
ENST00000494661.1:n.80-4809del
NM_001288973.1:c.340-4809del NP_001275902.1:n.340-4809del
NM_001288974.1:c.340-4809del NP_001275903.1:n.340-4809del
NM_001288975.1:c.340-4809del NP_001275904.1:n.340-4809del
NM_003474.5:c.349-4809del NP_003465.3:n.349-4809del
NM_021641.4:c.349-4809del NP_067673.2:n.349-4809del
XM_017016705.1:c.-120-4809del XP_016872194.1:n.-120-4809del
NM_001288973.2:c.340-4809del MANE Select NP_001275902.1:n.340-4809del
NM_001288974.2:c.340-4809del NP_001275903.1:n.340-4809del
NM_001288975.2:c.340-4809del NP_001275904.1:n.340-4809del
NM_003474.6:c.349-4809del NP_003465.3:n.349-4809del
NM_021641.5:c.349-4809del NP_067673.2:n.349-4809del