Canonical Allele Identifier: CA1943115817

Gene: ADAM12

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.126036121T= , CM000672.2:g.126036121T=	GRCh38
NC_000010.10:g.127724690T= , CM000672.1:g.127724690T=	GRCh37
NC_000010.9:g.127714680T=	NCBI36
NG_029050.1:g.357438A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448723.2:c.2529+25A= MANE Select	ENSP00000391268.2:n.2529+25A=
ENST00000368679.8:c.2538+25A=	ENSP00000357668.4:n.2538+25A=
NM_001288973.1:c.2529+25A=	NP_001275902.1:n.2529+25A=
NM_003474.5:c.2538+25A=	NP_003465.3:n.2538+25A=
XM_017016705.1:c.2070+25A=	XP_016872194.1:n.2070+25A=
XM_017016706.1:c.1371+25A=	XP_016872195.1:n.1371+25A=
XM_024448210.1:c.1200+25A=	XP_024303978.1:n.1200+25A=
NM_001288973.2:c.2529+25A= MANE Select	NP_001275902.1:n.2529+25A=
NM_003474.6:c.2538+25A=	NP_003465.3:n.2538+25A=