Canonical Allele Identifier: CA408103828
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669599C>G , CM000682.2:g.3669599C>G GRCh38
NC_000020.10:g.3650246C>G , CM000682.1:g.3650246C>G GRCh37
NC_000020.9:g.3598246C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2279G>C MANE Select ENSP00000348912.3:p.Gly760Ala
ENST00000350009.6:c.2201G>C ENSP00000322550.5:p.Gly734Ala
ENST00000356518.6:c.2279G>C ENSP00000348912.2:p.Gly760Ala
ENST00000379861.8:c.2279G>C ENSP00000369190.4:p.Gly760Ala
ENST00000466620.5:n.1840G>C
ENST00000483362.1:n.1027G>C
ENST00000617732.1:c.*966G>C ENSP00000483343.1:n.*966G>C
ENST00000619289.4:c.1919G>C ENSP00000484600.1:p.Gly640Ala
NM_001282447.1:c.2279G>C NP_001269376.1:p.Gly760Ala
NM_025220.3:c.2279G>C NP_079496.1:p.Gly760Ala
NM_153202.2:c.2201G>C NP_694882.1:p.Gly734Ala
XM_005260843.1:c.2318G>C XP_005260900.1:p.Gly773Ala
XM_006723639.1:c.2318G>C XP_006723702.1:p.Gly773Ala
XM_006723640.1:c.2309G>C XP_006723703.1:p.Gly770Ala
XM_011529366.1:c.2315G>C XP_011527668.1:p.Gly772Ala
XM_011529367.1:c.2276G>C XP_011527669.1:p.Gly759Ala
XM_011529368.1:c.2240G>C XP_011527670.1:p.Gly747Ala
XM_011529373.1:c.1316G>C XP_011527675.1:p.Gly439Ala
XR_937151.1:n.2384-229G>C
XR_937152.1:n.2384-229G>C
XR_937153.1:n.2303G>C
XR_937154.1:n.2303G>C
XR_937155.1:n.2224G>C
XR_937157.1:n.2226G>C
NM_001282447.2:c.2279G>C NP_001269376.1:p.Gly760Ala
NM_025220.4:c.2279G>C NP_079496.1:p.Gly760Ala
NM_153202.3:c.2201G>C NP_694882.1:p.Gly734Ala
XM_011529373.2:c.1316G>C XP_011527675.1:p.Gly439Ala
XR_001754405.1:n.2390G>C
XR_002958534.1:n.2499G>C
NM_001282447.3:c.2279G>C NP_001269376.1:p.Gly760Ala
NM_025220.5:c.2279G>C MANE Select NP_079496.1:p.Gly760Ala
NM_153202.4:c.2201G>C NP_694882.1:p.Gly734Ala