Canonical Allele Identifier: CA408103814

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669592G>C , CM000682.2:g.3669592G>C	GRCh38
NC_000020.10:g.3650239G>C , CM000682.1:g.3650239G>C	GRCh37
NC_000020.9:g.3598239G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025220.5:c.2286C>G MANE Select	NP_079496.1:p.His762Gln
ENST00000356518.7:c.2286C>G MANE Select	ENSP00000348912.3:p.His762Gln
NM_001282447.1:c.2286C>G	NP_001269376.1:p.His762Gln
NM_001282447.2:c.2286C>G	NP_001269376.1:p.His762Gln
NM_001282447.3:c.2286C>G	NP_001269376.1:p.His762Gln
NM_025220.3:c.2286C>G	NP_079496.1:p.His762Gln
NM_025220.4:c.2286C>G	NP_079496.1:p.His762Gln
NM_153202.2:c.2208C>G	NP_694882.1:p.His736Gln
NM_153202.3:c.2208C>G	NP_694882.1:p.His736Gln
NM_153202.4:c.2208C>G	NP_694882.1:p.His736Gln
ENST00000350009.6:c.2208C>G	ENSP00000322550.5:p.His736Gln
ENST00000356518.6:c.2286C>G	ENSP00000348912.2:p.His762Gln
ENST00000379861.8:c.2286C>G	ENSP00000369190.4:p.His762Gln
ENST00000466620.5:n.1847C>G
ENST00000483362.1:n.1034C>G
ENST00000617732.1:c.*973C>G	ENSP00000483343.1:n.*973C>G
ENST00000619289.4:c.1926C>G	ENSP00000484600.1:p.His642Gln
XM_005260843.1:c.2325C>G	XP_005260900.1:p.His775Gln
XM_006723639.1:c.2325C>G	XP_006723702.1:p.His775Gln
XM_006723640.1:c.2316C>G	XP_006723703.1:p.His772Gln
XM_011529366.1:c.2322C>G	XP_011527668.1:p.His774Gln
XM_011529367.1:c.2283C>G	XP_011527669.1:p.His761Gln
XM_011529368.1:c.2247C>G	XP_011527670.1:p.His749Gln
XM_011529373.1:c.1323C>G	XP_011527675.1:p.His441Gln
XM_011529373.2:c.1323C>G	XP_011527675.1:p.His441Gln
XR_001754405.1:n.2397C>G
XR_002958534.1:n.2506C>G
XR_937151.1:n.2384-222C>G
XR_937152.1:n.2384-222C>G
XR_937153.1:n.2310C>G
XR_937154.1:n.2310C>G
XR_937155.1:n.2231C>G
XR_937157.1:n.2233C>G