Canonical Allele Identifier: CA10630989

Gene: ADAM9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.39017312C>T , CM000670.2:g.39017312C>T	GRCh38
NC_000008.10:g.38874831C>T , CM000670.1:g.38874831C>T	GRCh37
NC_000008.9:g.38993988C>T	NCBI36
NG_016335.1:g.25327C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481058.2:n.654C>T
ENST00000487273.7:c.504C>T MANE Select	ENSP00000419446.2:p.Val168=
ENST00000676489.1:n.1617C>T
ENST00000676617.1:c.504C>T	ENSP00000504583.1:p.Val168=
ENST00000676643.1:c.504C>T	ENSP00000503079.1:p.Val168=
ENST00000676669.1:c.504C>T	ENSP00000503215.1:p.Val168=
ENST00000676765.1:c.504C>T	ENSP00000503374.1:p.Val168=
ENST00000676919.1:n.1625C>T
ENST00000676936.1:c.504C>T	ENSP00000504471.1:p.Val168=
ENST00000677004.1:c.504C>T	ENSP00000503932.1:p.Val168=
ENST00000677137.1:c.504C>T	ENSP00000502895.1:p.Val168=
ENST00000677165.1:c.504C>T	ENSP00000502865.1:p.Val168=
ENST00000677359.1:c.504C>T	ENSP00000504373.1:p.Val168=
ENST00000677582.1:c.504C>T	ENSP00000503648.1:p.Val168=
ENST00000677908.1:c.504C>T	ENSP00000504640.1:p.Val168=
ENST00000678253.1:c.*235C>T	ENSP00000503454.1:n.*235C>T
ENST00000678474.1:c.504C>T	ENSP00000503418.1:p.Val168=
ENST00000678540.1:c.504C>T	ENSP00000503206.1:p.Val168=
ENST00000678730.1:c.*235C>T	ENSP00000503523.1:n.*235C>T
ENST00000679268.1:c.504C>T	ENSP00000503584.1:p.Val168=
ENST00000379917.7:c.504C>T	ENSP00000369249.3:p.Val168=
ENST00000468065.5:c.504C>T	ENSP00000418737.1:p.Val168=
ENST00000481058.1:n.277C>T
ENST00000481873.7:c.504C>T	ENSP00000418437.3:p.Val168=
ENST00000487273.6:c.504C>T	ENSP00000419446.2:p.Val168=
NM_003816.2:c.504C>T	NP_003807.1:p.Val168=
NR_027638.1:n.582C>T
NR_027639.1:n.582C>T
NR_027878.1:n.582C>T
XM_011544682.1:c.450C>T	XP_011542984.1:p.Val150=
XR_949497.1:n.603C>T
XM_011544682.2:c.450C>T	XP_011542984.1:p.Val150=
XM_017013942.1:c.510C>T	XP_016869431.1:p.Val170=
XR_001745615.1:n.525C>T
XR_001745616.2:n.801C>T
XR_001745617.1:n.4961C>T
XR_001745618.2:n.801C>T
NM_003816.3:c.504C>T MANE Select	NP_003807.1:p.Val168=
NR_027638.2:n.595C>T
NR_027639.2:n.595C>T
NR_027878.2:n.595C>T