Canonical Allele Identifier: CA408103850

Gene: ADAM33

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669611T>A , CM000682.2:g.3669611T>A	GRCh38
NC_000020.10:g.3650258T>A , CM000682.1:g.3650258T>A	GRCh37
NC_000020.9:g.3598258T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2267A>T MANE Select	ENSP00000348912.3:p.His756Leu
ENST00000350009.6:c.2189A>T	ENSP00000322550.5:p.His730Leu
ENST00000356518.6:c.2267A>T	ENSP00000348912.2:p.His756Leu
ENST00000379861.8:c.2267A>T	ENSP00000369190.4:p.His756Leu
ENST00000466620.5:n.1828A>T
ENST00000483362.1:n.1015A>T
ENST00000617732.1:c.*954A>T	ENSP00000483343.1:n.*954A>T
ENST00000619289.4:c.1907A>T	ENSP00000484600.1:p.His636Leu
NM_001282447.1:c.2267A>T	NP_001269376.1:p.His756Leu
NM_025220.3:c.2267A>T	NP_079496.1:p.His756Leu
NM_153202.2:c.2189A>T	NP_694882.1:p.His730Leu
XM_005260843.1:c.2306A>T	XP_005260900.1:p.His769Leu
XM_006723639.1:c.2306A>T	XP_006723702.1:p.His769Leu
XM_006723640.1:c.2297A>T	XP_006723703.1:p.His766Leu
XM_011529366.1:c.2303A>T	XP_011527668.1:p.His768Leu
XM_011529367.1:c.2264A>T	XP_011527669.1:p.His755Leu
XM_011529368.1:c.2228A>T	XP_011527670.1:p.His743Leu
XM_011529373.1:c.1304A>T	XP_011527675.1:p.His435Leu
XR_937151.1:n.2384-241A>T
XR_937152.1:n.2384-241A>T
XR_937153.1:n.2291A>T
XR_937154.1:n.2291A>T
XR_937155.1:n.2212A>T
XR_937157.1:n.2214A>T
NM_001282447.2:c.2267A>T	NP_001269376.1:p.His756Leu
NM_025220.4:c.2267A>T	NP_079496.1:p.His756Leu
NM_153202.3:c.2189A>T	NP_694882.1:p.His730Leu
XM_011529373.2:c.1304A>T	XP_011527675.1:p.His435Leu
XR_001754405.1:n.2378A>T
XR_002958534.1:n.2487A>T
NM_001282447.3:c.2267A>T	NP_001269376.1:p.His756Leu
NM_025220.5:c.2267A>T MANE Select	NP_079496.1:p.His756Leu
NM_153202.4:c.2189A>T	NP_694882.1:p.His730Leu