Canonical Allele Identifier: CA4721177

Gene: ADAM9 TM2D2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.38997078G>A , CM000670.2:g.38997078G>A	GRCh38
NC_000008.10:g.38854597G>A , CM000670.1:g.38854597G>A	GRCh37
NC_000008.9:g.38973754G>A	NCBI36
NG_016335.1:g.5093G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481058.2:n.165G>A (ADAM9)
ENST00000487273.7:c.15G>A (ADAM9) MANE Select	ENSP00000419446.2:p.Ala5=
ENST00000676489.1:n.104G>A (ADAM9)
ENST00000676617.1:c.15G>A (ADAM9)	ENSP00000504583.1:p.Ala5=
ENST00000676643.1:c.15G>A (ADAM9)	ENSP00000503079.1:p.Ala5=
ENST00000676669.1:c.15G>A (ADAM9)	ENSP00000503215.1:p.Ala5=
ENST00000676765.1:c.15G>A (ADAM9)	ENSP00000503374.1:p.Ala5=
ENST00000676936.1:c.15G>A (ADAM9)	ENSP00000504471.1:p.Ala5=
ENST00000677004.1:c.15G>A (ADAM9)	ENSP00000503932.1:p.Ala5=
ENST00000677137.1:c.15G>A (ADAM9)	ENSP00000502895.1:p.Ala5=
ENST00000677165.1:c.15G>A (ADAM9)	ENSP00000502865.1:p.Ala5=
ENST00000677359.1:c.15G>A (ADAM9)	ENSP00000504373.1:p.Ala5=
ENST00000677582.1:c.15G>A (ADAM9)	ENSP00000503648.1:p.Ala5=
ENST00000677908.1:c.15G>A (ADAM9)	ENSP00000504640.1:p.Ala5=
ENST00000678253.1:c.15G>A (ADAM9)	ENSP00000503454.1:p.Ala5=
ENST00000678474.1:c.15G>A (ADAM9)	ENSP00000503418.1:p.Ala5=
ENST00000678540.1:c.15G>A (ADAM9)	ENSP00000503206.1:p.Ala5=
ENST00000678730.1:c.15G>A (ADAM9)	ENSP00000503523.1:p.Ala5=
ENST00000679268.1:c.15G>A (ADAM9)	ENSP00000503584.1:p.Ala5=
ENST00000379917.7:c.15G>A (ADAM9)	ENSP00000369249.3:p.Ala5=
ENST00000466936.5:c.15G>A (ADAM9)	ENSP00000420257.1:p.Ala5=
ENST00000468065.5:c.15G>A (ADAM9)	ENSP00000418737.1:p.Ala5=
ENST00000481513.5:c.15G>A (ADAM9)	ENSP00000417066.1:p.Ala5=
ENST00000481873.7:c.15G>A (ADAM9)	ENSP00000418437.3:p.Ala5=
ENST00000487273.6:c.15G>A (ADAM9)	ENSP00000419446.2:p.Ala5=
NM_003816.2:c.15G>A (ADAM9)	NP_003807.1:p.Ala5=
NR_027638.1:n.93G>A (ADAM9)
NR_027639.1:n.93G>A (ADAM9)
NR_027878.1:n.93G>A (ADAM9)
XR_949497.1:n.114G>A (ADAM9)
XM_011544667.2:c.-676C>T (TM2D2)	XP_011542969.1:n.-676C>T
XR_001745616.2:n.312G>A (ADAM9)
XR_001745618.2:n.312G>A (ADAM9)
NM_003816.3:c.15G>A (ADAM9) MANE Select	NP_003807.1:p.Ala5=
NR_027638.2:n.106G>A (ADAM9)
NR_027639.2:n.106G>A (ADAM9)
NR_027878.2:n.106G>A (ADAM9)