Canonical Allele Identifier: CA2611381693

Gene: ADAM12

Linked Data

• gnomAD v4: 10-126036113-CTACATCCTATCATATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126036114_126036129del , CM000672.2:g.126036114_126036129del	GRCh38
NC_000010.10:g.127724683_127724698del , CM000672.1:g.127724683_127724698del	GRCh37
NC_000010.9:g.127714673_127714688del	NCBI36
NG_029050.1:g.357430_357445del

Transcript Alleles

HGVS	Amino-acid change
ENST00000448723.2:c.2529+17_2529+32del MANE Select	ENSP00000391268.2:n.2529+17_2529+32del
ENST00000368679.8:c.2538+17_2538+32del	ENSP00000357668.4:n.2538+17_2538+32del
NM_001288973.1:c.2529+17_2529+32del	NP_001275902.1:n.2529+17_2529+32del
NM_003474.5:c.2538+17_2538+32del	NP_003465.3:n.2538+17_2538+32del
XM_017016705.1:c.2070+17_2070+32del	XP_016872194.1:n.2070+17_2070+32del
XM_017016706.1:c.1371+17_1371+32del	XP_016872195.1:n.1371+17_1371+32del
XM_024448210.1:c.1200+17_1200+32del	XP_024303978.1:n.1200+17_1200+32del
NM_001288973.2:c.2529+17_2529+32del MANE Select	NP_001275902.1:n.2529+17_2529+32del
NM_003474.6:c.2538+17_2538+32del	NP_003465.3:n.2538+17_2538+32del