Canonical Allele Identifier: CA4678595

Gene: ADAM28 ADAM7-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.24326627G>A , CM000670.2:g.24326627G>A	GRCh38
NC_000008.10:g.24184140G>A , CM000670.1:g.24184140G>A	GRCh37
NC_000008.9:g.24240085G>A	NCBI36
NG_029394.2:g.37561G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699027.1:c.964G>A (ADAM28)	ENSP00000514095.1:p.Val322Ile
ENST00000265769.9:c.964G>A (ADAM28) MANE Select	ENSP00000265769.4:p.Val322Ile
ENST00000265769.8:c.964G>A (ADAM28)	ENSP00000265769.4:p.Val322Ile
ENST00000437154.6:c.964G>A (ADAM28)	ENSP00000393699.2:p.Val322Ile
ENST00000518516.5:n.298G>A (ADAM28)
ENST00000520448.5:c.*372G>A (ADAM28)	ENSP00000430085.1:n.*372G>A
ENST00000521110.1:n.127G>A (ADAM28)
NM_001304351.1:c.964G>A (ADAM28)	NP_001291280.1:p.Val322Ile
NM_014265.5:c.964G>A (ADAM28)	NP_055080.2:p.Val322Ile
NM_021777.4:c.964G>A (ADAM28)	NP_068547.2:p.Val322Ile
NR_125808.1:n.502-25698C>T (ADAM7-AS1)
NR_130709.1:n.881G>A (ADAM28)
NR_130710.1:n.1136G>A (ADAM28)
XM_005273380.2:c.964G>A (ADAM28)	XP_005273437.1:p.Val322Ile
XM_005273382.1:c.964G>A (ADAM28)	XP_005273439.1:p.Val322Ile
XM_006716273.2:c.964G>A (ADAM28)	XP_006716336.1:p.Val322Ile
XM_006716274.1:c.964G>A (ADAM28)	XP_006716337.1:p.Val322Ile
XM_006716275.2:c.694G>A (ADAM28)	XP_006716338.1:p.Val232Ile
XM_011544366.1:c.961G>A (ADAM28)	XP_011542668.1:p.Val321Ile
XM_011544367.1:c.964G>A (ADAM28)	XP_011542669.1:p.Val322Ile
XM_011544368.1:c.964G>A (ADAM28)	XP_011542670.1:p.Val322Ile
XM_011544369.1:c.964G>A (ADAM28)	XP_011542671.1:p.Val322Ile
XM_011544370.1:c.265G>A (ADAM28)	XP_011542672.1:p.Val89Ile
XM_011544371.1:c.205G>A (ADAM28)	XP_011542673.1:p.Val69Ile
XR_247120.2:n.1074G>A (ADAM28)
XR_949375.1:n.1074G>A (ADAM28)
XM_005273380.4:c.964G>A (ADAM28)	XP_005273437.1:p.Val322Ile
XM_006716273.3:c.964G>A (ADAM28)	XP_006716336.1:p.Val322Ile
XM_011544367.3:c.964G>A (ADAM28)	XP_011542669.1:p.Val322Ile
XM_011544368.3:c.964G>A (ADAM28)	XP_011542670.1:p.Val322Ile
XM_011544369.2:c.964G>A (ADAM28)	XP_011542671.1:p.Val322Ile
XM_011544370.2:c.265G>A (ADAM28)	XP_011542672.1:p.Val89Ile
XM_011544371.3:c.205G>A (ADAM28)	XP_011542673.1:p.Val69Ile
XM_017012974.2:c.964G>A (ADAM28)	XP_016868463.1:p.Val322Ile
XM_017012975.2:c.964G>A (ADAM28)	XP_016868464.1:p.Val322Ile
XM_017012976.1:c.784G>A (ADAM28)	XP_016868465.1:p.Val262Ile
XR_247120.3:n.1074G>A (ADAM28)
XR_949375.3:n.1074G>A (ADAM28)
NM_001304351.2:c.964G>A (ADAM28)	NP_001291280.1:p.Val322Ile
NM_014265.6:c.964G>A (ADAM28) MANE Select	NP_055080.2:p.Val322Ile
NR_130710.2:n.1107G>A (ADAM28)
NM_021777.5:c.964G>A (ADAM28)	NP_068547.2:p.Val322Ile
NR_130709.2:n.852G>A (ADAM28)