Canonical Allele Identifier: CA661284430

Gene: ADAM12

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126158100C>G , CM000672.2:g.126158100C>G	GRCh38
NC_000010.10:g.127846669C>G , CM000672.1:g.127846669C>G	GRCh37
NC_000010.9:g.127836659C>G	NCBI36
NG_029050.1:g.235459G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448723.2:c.261-2795G>C MANE Select	ENSP00000391268.2:n.261-2795G>C
ENST00000368676.8:c.261-2795G>C	ENSP00000357665.4:n.261-2795G>C
ENST00000368679.8:c.261-2795G>C	ENSP00000357668.4:n.261-2795G>C
ENST00000448723.1:c.261-2795G>C	ENSP00000391268.1:n.261-2795G>C
NM_001288973.1:c.261-2795G>C	NP_001275902.1:n.261-2795G>C
NM_001288974.1:c.261-2795G>C	NP_001275903.1:n.261-2795G>C
NM_001288975.1:c.261-2795G>C	NP_001275904.1:n.261-2795G>C
NM_003474.5:c.261-2795G>C	NP_003465.3:n.261-2795G>C
NM_021641.4:c.261-2795G>C	NP_067673.2:n.261-2795G>C
XM_017016705.1:c.-199-2795G>C	XP_016872194.1:n.-199-2795G>C
NM_001288973.2:c.261-2795G>C MANE Select	NP_001275902.1:n.261-2795G>C
NM_001288974.2:c.261-2795G>C	NP_001275903.1:n.261-2795G>C
NM_001288975.2:c.261-2795G>C	NP_001275904.1:n.261-2795G>C
NM_003474.6:c.261-2795G>C	NP_003465.3:n.261-2795G>C
NM_021641.5:c.261-2795G>C	NP_067673.2:n.261-2795G>C