Canonical Allele Identifier: CA2611381696

Gene: ADAM12

Linked Data

• gnomAD v4: 10-126036116-C-CATCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126036120_126036124dup , CM000672.2:g.126036120_126036124dup	GRCh38
NC_000010.10:g.127724689_127724693dup , CM000672.1:g.127724689_127724693dup	GRCh37
NC_000010.9:g.127714679_127714683dup	NCBI36
NG_029050.1:g.357438_357442dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000448723.2:c.2529+25_2529+29dup MANE Select	ENSP00000391268.2:n.2529+25_2529+29dup
ENST00000368679.8:c.2538+25_2538+29dup	ENSP00000357668.4:n.2538+25_2538+29dup
NM_001288973.1:c.2529+25_2529+29dup	NP_001275902.1:n.2529+25_2529+29dup
NM_003474.5:c.2538+25_2538+29dup	NP_003465.3:n.2538+25_2538+29dup
XM_017016705.1:c.2070+25_2070+29dup	XP_016872194.1:n.2070+25_2070+29dup
XM_017016706.1:c.1371+25_1371+29dup	XP_016872195.1:n.1371+25_1371+29dup
XM_024448210.1:c.1200+25_1200+29dup	XP_024303978.1:n.1200+25_1200+29dup
NM_001288973.2:c.2529+25_2529+29dup MANE Select	NP_001275902.1:n.2529+25_2529+29dup
NM_003474.6:c.2538+25_2538+29dup	NP_003465.3:n.2538+25_2538+29dup