Canonical Allele Identifier: CA460407168

Gene: ADAM9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.39017243G>T , CM000670.2:g.39017243G>T	GRCh38
NC_000008.10:g.38874762G>T , CM000670.1:g.38874762G>T	GRCh37
NC_000008.9:g.38993919G>T	NCBI36
NG_016335.1:g.25258G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481058.2:n.585G>T
ENST00000487273.7:c.435G>T MANE Select	ENSP00000419446.2:p.Ala145=
ENST00000676489.1:n.1548G>T
ENST00000676617.1:c.435G>T	ENSP00000504583.1:p.Ala145=
ENST00000676643.1:c.435G>T	ENSP00000503079.1:p.Ala145=
ENST00000676669.1:c.435G>T	ENSP00000503215.1:p.Ala145=
ENST00000676765.1:c.435G>T	ENSP00000503374.1:p.Ala145=
ENST00000676919.1:n.1556G>T
ENST00000676936.1:c.435G>T	ENSP00000504471.1:p.Ala145=
ENST00000677004.1:c.435G>T	ENSP00000503932.1:p.Ala145=
ENST00000677137.1:c.435G>T	ENSP00000502895.1:p.Ala145=
ENST00000677165.1:c.435G>T	ENSP00000502865.1:p.Ala145=
ENST00000677359.1:c.435G>T	ENSP00000504373.1:p.Ala145=
ENST00000677582.1:c.435G>T	ENSP00000503648.1:p.Ala145=
ENST00000677908.1:c.435G>T	ENSP00000504640.1:p.Ala145=
ENST00000678253.1:c.*166G>T	ENSP00000503454.1:n.*166G>T
ENST00000678474.1:c.435G>T	ENSP00000503418.1:p.Ala145=
ENST00000678540.1:c.435G>T	ENSP00000503206.1:p.Ala145=
ENST00000678730.1:c.*166G>T	ENSP00000503523.1:n.*166G>T
ENST00000679268.1:c.435G>T	ENSP00000503584.1:p.Ala145=
ENST00000379917.7:c.435G>T	ENSP00000369249.3:p.Ala145=
ENST00000468065.5:c.435G>T	ENSP00000418737.1:p.Ala145=
ENST00000481058.1:n.208G>T
ENST00000481873.7:c.435G>T	ENSP00000418437.3:p.Ala145=
ENST00000487273.6:c.435G>T	ENSP00000419446.2:p.Ala145=
NM_003816.2:c.435G>T	NP_003807.1:p.Ala145=
NR_027638.1:n.513G>T
NR_027639.1:n.513G>T
NR_027878.1:n.513G>T
XM_011544682.1:c.381G>T	XP_011542984.1:p.Ala127=
XR_949497.1:n.534G>T
XM_011544682.2:c.381G>T	XP_011542984.1:p.Ala127=
XM_017013942.1:c.441G>T	XP_016869431.1:p.Ala147=
XR_001745615.1:n.456G>T
XR_001745616.2:n.732G>T
XR_001745617.1:n.4892G>T
XR_001745618.2:n.732G>T
NM_003816.3:c.435G>T MANE Select	NP_003807.1:p.Ala145=
NR_027638.2:n.526G>T
NR_027639.2:n.526G>T
NR_027878.2:n.526G>T