Canonical Allele Identifier: CA4721216

Gene: ADAM9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.39007903C>T , CM000670.2:g.39007903C>T	GRCh38
NC_000008.10:g.38865422C>T , CM000670.1:g.38865422C>T	GRCh37
NC_000008.9:g.38984579C>T	NCBI36
NG_016335.1:g.15918C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000481058.2:n.265C>T
ENST00000487273.7:c.115C>T MANE Select	ENSP00000419446.2:p.His39Tyr
ENST00000676489.1:n.204C>T
ENST00000676617.1:c.115C>T	ENSP00000504583.1:p.His39Tyr
ENST00000676643.1:c.115C>T	ENSP00000503079.1:p.His39Tyr
ENST00000676669.1:c.115C>T	ENSP00000503215.1:p.His39Tyr
ENST00000676765.1:c.115C>T	ENSP00000503374.1:p.His39Tyr
ENST00000676919.1:n.1295C>T
ENST00000676936.1:c.115C>T	ENSP00000504471.1:p.His39Tyr
ENST00000677004.1:c.115C>T	ENSP00000503932.1:p.His39Tyr
ENST00000677137.1:c.115C>T	ENSP00000502895.1:p.His39Tyr
ENST00000677165.1:c.115C>T	ENSP00000502865.1:p.His39Tyr
ENST00000677359.1:c.115C>T	ENSP00000504373.1:p.His39Tyr
ENST00000677582.1:c.115C>T	ENSP00000503648.1:p.His39Tyr
ENST00000677908.1:c.115C>T	ENSP00000504640.1:p.His39Tyr
ENST00000678253.1:c.115C>T	ENSP00000503454.1:p.His39Tyr
ENST00000678474.1:c.115C>T	ENSP00000503418.1:p.His39Tyr
ENST00000678540.1:c.115C>T	ENSP00000503206.1:p.His39Tyr
ENST00000678730.1:c.115C>T	ENSP00000503523.1:p.His39Tyr
ENST00000679268.1:c.115C>T	ENSP00000503584.1:p.His39Tyr
ENST00000379917.7:c.115C>T	ENSP00000369249.3:p.His39Tyr
ENST00000466936.5:c.115C>T	ENSP00000420257.1:p.His39Tyr
ENST00000468065.5:c.115C>T	ENSP00000418737.1:p.His39Tyr
ENST00000481513.5:c.115C>T	ENSP00000417066.1:p.His39Tyr
ENST00000481873.7:c.115C>T	ENSP00000418437.3:p.His39Tyr
ENST00000487273.6:c.115C>T	ENSP00000419446.2:p.His39Tyr
NM_003816.2:c.115C>T	NP_003807.1:p.His39Tyr
NR_027638.1:n.193C>T
NR_027639.1:n.193C>T
NR_027878.1:n.193C>T
XM_011544682.1:c.61C>T	XP_011542984.1:p.His21Tyr
XR_949497.1:n.214C>T
XM_011544682.2:c.61C>T	XP_011542984.1:p.His21Tyr
XM_017013942.1:c.121C>T	XP_016869431.1:p.His41Tyr
XR_001745615.1:n.136C>T
XR_001745616.2:n.412C>T
XR_001745617.1:n.4572C>T
XR_001745618.2:n.412C>T
NM_003816.3:c.115C>T MANE Select	NP_003807.1:p.His39Tyr
NR_027638.2:n.206C>T
NR_027639.2:n.206C>T
NR_027878.2:n.206C>T