Canonical Allele Identifier: CA199510

Gene: ADAM9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.39055575A>G , CM000670.2:g.39055575A>G	GRCh38
NC_000008.10:g.38913094A>G , CM000670.1:g.38913094A>G	GRCh37
NC_000008.9:g.39032251A>G	NCBI36
NG_016335.1:g.63590A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481058.2:n.4270-2A>G
ENST00000487273.7:c.1396-2A>G MANE Select	ENSP00000419446.2:n.1396-2A>G
ENST00000676489.1:n.2509-2A>G
ENST00000676617.1:c.1396-2A>G	ENSP00000504583.1:n.1396-2A>G
ENST00000676643.1:c.1396-2A>G	ENSP00000503079.1:n.1396-2A>G
ENST00000676669.1:c.1396-2A>G	ENSP00000503215.1:n.1396-2A>G
ENST00000676765.1:c.1396-2A>G	ENSP00000503374.1:n.1396-2A>G
ENST00000676919.1:n.2517-2A>G
ENST00000676936.1:c.*714-2A>G	ENSP00000504471.1:n.*714-2A>G
ENST00000677004.1:c.1489-2A>G	ENSP00000503932.1:n.1489-2A>G
ENST00000677137.1:c.1396-2A>G	ENSP00000502895.1:n.1396-2A>G
ENST00000677165.1:c.1396-2A>G	ENSP00000502865.1:n.1396-2A>G
ENST00000677359.1:c.1396-2A>G	ENSP00000504373.1:n.1396-2A>G
ENST00000677582.1:c.1396-2A>G	ENSP00000503648.1:n.1396-2A>G
ENST00000677908.1:c.1224-2A>G	ENSP00000504640.1:n.1224-2A>G
ENST00000678253.1:c.*1127-2A>G	ENSP00000503454.1:n.*1127-2A>G
ENST00000678474.1:c.1396-2A>G	ENSP00000503418.1:n.1396-2A>G
ENST00000678540.1:c.*112-2A>G	ENSP00000503206.1:n.*112-2A>G
ENST00000678730.1:c.*1127-2A>G	ENSP00000503523.1:n.*1127-2A>G
ENST00000678863.1:c.171-2A>G	ENSP00000503906.1:n.171-2A>G
ENST00000679268.1:c.*112-2A>G	ENSP00000503584.1:n.*112-2A>G
ENST00000379917.7:c.1396-2A>G	ENSP00000369249.3:n.1396-2A>G
ENST00000468065.5:c.1396-2A>G	ENSP00000418737.1:n.1396-2A>G
ENST00000481873.7:c.1396-2A>G	ENSP00000418437.3:n.1396-2A>G
ENST00000487273.6:c.1396-2A>G	ENSP00000419446.2:n.1396-2A>G
NM_003816.2:c.1396-2A>G	NP_003807.1:n.1396-2A>G
NR_027638.1:n.1474-2A>G
NR_027639.1:n.1474-2A>G
NR_027878.1:n.1474-2A>G
XM_011544682.1:c.1342-2A>G	XP_011542984.1:n.1342-2A>G
XR_949497.1:n.1495-2A>G
XM_011544682.2:c.1342-2A>G	XP_011542984.1:n.1342-2A>G
XM_017013942.1:c.1402-2A>G	XP_016869431.1:n.1402-2A>G
XR_001745615.1:n.1417-2A>G
XR_001745616.2:n.1693-2A>G
XR_001745617.1:n.5853-2A>G
XR_001745618.2:n.1693-2A>G
NM_003816.3:c.1396-2A>G MANE Select	NP_003807.1:n.1396-2A>G
NR_027638.2:n.1487-2A>G
NR_027639.2:n.1487-2A>G
NR_027878.2:n.1487-2A>G