Canonical Allele Identifier: CA4721384
Gene: ADAM9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.39018835T>C , CM000670.2:g.39018835T>C GRCh38
NC_000008.10:g.38876354T>C , CM000670.1:g.38876354T>C GRCh37
NC_000008.9:g.38995511T>C NCBI36
NG_016335.1:g.26850T>C

Transcript Alleles

HGVS Amino-acid Change
NM_003816.3:c.607-18T>C MANE Select NP_003807.1:n.607-18T>C
ENST00000487273.7:c.607-18T>C MANE Select ENSP00000419446.2:n.607-18T>C
NM_003816.2:c.607-18T>C NP_003807.1:n.607-18T>C
NR_027638.1:n.685-18T>C
NR_027638.2:n.698-18T>C
NR_027639.1:n.685-18T>C
NR_027639.2:n.698-18T>C
NR_027878.1:n.685-18T>C
NR_027878.2:n.698-18T>C
ENST00000379917.7:c.607-18T>C ENSP00000369249.3:n.607-18T>C
ENST00000468065.5:c.607-18T>C ENSP00000418737.1:n.607-18T>C
ENST00000481058.1:n.380-18T>C
ENST00000481058.2:n.757-18T>C
ENST00000481873.7:c.607-18T>C ENSP00000418437.3:n.607-18T>C
ENST00000487273.6:c.607-18T>C ENSP00000419446.2:n.607-18T>C
ENST00000676489.1:n.1720-18T>C
ENST00000676617.1:c.607-18T>C ENSP00000504583.1:n.607-18T>C
ENST00000676643.1:c.607-18T>C ENSP00000503079.1:n.607-18T>C
ENST00000676669.1:c.607-18T>C ENSP00000503215.1:n.607-18T>C
ENST00000676765.1:c.607-18T>C ENSP00000503374.1:n.607-18T>C
ENST00000676919.1:n.1728-18T>C
ENST00000676936.1:c.607-18T>C ENSP00000504471.1:n.607-18T>C
ENST00000677004.1:c.607-18T>C ENSP00000503932.1:n.607-18T>C
ENST00000677137.1:c.607-18T>C ENSP00000502895.1:n.607-18T>C
ENST00000677165.1:c.607-18T>C ENSP00000502865.1:n.607-18T>C
ENST00000677359.1:c.607-18T>C ENSP00000504373.1:n.607-18T>C
ENST00000677582.1:c.607-18T>C ENSP00000503648.1:n.607-18T>C
ENST00000677908.1:c.607-18T>C ENSP00000504640.1:n.607-18T>C
ENST00000678253.1:c.*338-18T>C ENSP00000503454.1:n.*338-18T>C
ENST00000678474.1:c.607-18T>C ENSP00000503418.1:n.607-18T>C
ENST00000678540.1:c.607-18T>C ENSP00000503206.1:n.607-18T>C
ENST00000678730.1:c.*338-18T>C ENSP00000503523.1:n.*338-18T>C
ENST00000679268.1:c.607-18T>C ENSP00000503584.1:n.607-18T>C
XM_011544682.1:c.553-18T>C XP_011542984.1:n.553-18T>C
XM_011544682.2:c.553-18T>C XP_011542984.1:n.553-18T>C
XM_017013942.1:c.613-18T>C XP_016869431.1:n.613-18T>C
XR_001745615.1:n.628-18T>C
XR_001745616.2:n.904-18T>C
XR_001745617.1:n.5064-18T>C
XR_001745618.2:n.904-18T>C
XR_949497.1:n.706-18T>C