Canonical Allele Identifier: CA634188031

Gene: ADAM33

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668421G>A , CM000682.2:g.3668421G>A	GRCh38
NC_000020.10:g.3649068G>A , CM000682.1:g.3649068G>A	GRCh37
NC_000020.9:g.3597068G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.*542C>T MANE Select	ENSP00000348912.3:n.*542C>T
ENST00000350009.6:c.*542C>T	ENSP00000322550.5:n.*542C>T
ENST00000356518.6:c.*542C>T	ENSP00000348912.2:n.*542C>T
ENST00000379861.8:c.*542C>T	ENSP00000369190.4:n.*542C>T
ENST00000466620.5:n.2545C>T
ENST00000483362.1:n.1907C>T
ENST00000619289.4:c.*542C>T	ENSP00000484600.1:n.*542C>T
NM_001282447.1:c.*542C>T	NP_001269376.1:n.*542C>T
NM_025220.3:c.*542C>T	NP_079496.1:n.*542C>T
NM_153202.2:c.*542C>T	NP_694882.1:n.*542C>T
XM_005260843.1:c.*542C>T	XP_005260900.1:n.*542C>T
XM_006723639.1:c.*542C>T	XP_006723702.1:n.*542C>T
XM_006723640.1:c.*542C>T	XP_006723703.1:n.*542C>T
XM_011529366.1:c.*542C>T	XP_011527668.1:n.*542C>T
XM_011529367.1:c.*542C>T	XP_011527669.1:n.*542C>T
XM_011529368.1:c.*542C>T	XP_011527670.1:n.*542C>T
XM_011529373.1:c.*542C>T	XP_011527675.1:n.*542C>T
XR_937153.1:n.3005C>T
XR_937154.1:n.3005C>T
XR_937155.1:n.2926C>T
XR_937157.1:n.2928C>T
NM_001282447.2:c.*542C>T	NP_001269376.1:n.*542C>T
NM_025220.4:c.*542C>T	NP_079496.1:n.*542C>T
NM_153202.3:c.*542C>T	NP_694882.1:n.*542C>T
XM_011529373.2:c.*542C>T	XP_011527675.1:n.*542C>T
XR_001754405.1:n.3092C>T
XR_002958534.1:n.3201C>T
NM_001282447.3:c.*542C>T	NP_001269376.1:n.*542C>T
NM_025220.5:c.*542C>T MANE Select	NP_079496.1:n.*542C>T
NM_153202.4:c.*542C>T	NP_694882.1:n.*542C>T