Canonical Allele Identifier: CA13173775

Gene: ADAM12

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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