Canonical Allele Identifier: CA215379801

Gene: ADAM12

Linked Data

• dbSNP Id: rs978952994
• gnomAD v2: 10-127829108-G-T
• gnomAD v3: 10-126140539-G-T
• gnomAD v4: 10-126140539-G-T
• MyVariant Identifiers: chr10:g.127829108G>T (hg19) ; chr10:g.126140539G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126140539G>T , CM000672.2:g.126140539G>T	GRCh38
NC_000010.10:g.127829108G>T , CM000672.1:g.127829108G>T	GRCh37
NC_000010.9:g.127819098G>T	NCBI36
NG_029050.1:g.253020C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448723.2:c.340-4879C>A MANE Select	ENSP00000391268.2:n.340-4879C>A
ENST00000368676.8:c.349-4879C>A	ENSP00000357665.4:n.349-4879C>A
ENST00000368679.8:c.349-4879C>A	ENSP00000357668.4:n.349-4879C>A
ENST00000448723.1:c.340-4879C>A	ENSP00000391268.1:n.340-4879C>A
ENST00000494661.1:n.80-4879C>A
NM_001288973.1:c.340-4879C>A	NP_001275902.1:n.340-4879C>A
NM_001288974.1:c.340-4879C>A	NP_001275903.1:n.340-4879C>A
NM_001288975.1:c.340-4879C>A	NP_001275904.1:n.340-4879C>A
NM_003474.5:c.349-4879C>A	NP_003465.3:n.349-4879C>A
NM_021641.4:c.349-4879C>A	NP_067673.2:n.349-4879C>A
XM_017016705.1:c.-120-4879C>A	XP_016872194.1:n.-120-4879C>A
NM_001288973.2:c.340-4879C>A MANE Select	NP_001275902.1:n.340-4879C>A
NM_001288974.2:c.340-4879C>A	NP_001275903.1:n.340-4879C>A
NM_001288975.2:c.340-4879C>A	NP_001275904.1:n.340-4879C>A
NM_003474.6:c.349-4879C>A	NP_003465.3:n.349-4879C>A
NM_021641.5:c.349-4879C>A	NP_067673.2:n.349-4879C>A