Canonical Allele Identifier: CA408103427
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668977A>G , CM000682.2:g.3668977A>G GRCh38
NC_000020.10:g.3649624A>G , CM000682.1:g.3649624A>G GRCh37
NC_000020.9:g.3597624A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.7:c.2428T>C MANE Select ENSP00000348912.3:p.Ser810Pro
ENST00000350009.6:c.2350T>C ENSP00000322550.5:p.Ser784Pro
ENST00000356518.6:c.2428T>C ENSP00000348912.2:p.Ser810Pro
ENST00000379861.8:c.2425T>C ENSP00000369190.4:p.Ser809Pro
ENST00000466620.5:n.1989T>C
ENST00000483362.1:n.1351T>C
ENST00000617732.1:c.*1112T>C ENSP00000483343.1:n.*1112T>C
ENST00000619289.4:c.2065T>C ENSP00000484600.1:p.Ser689Pro
NM_001282447.1:c.2425T>C NP_001269376.1:p.Ser809Pro
NM_025220.3:c.2428T>C NP_079496.1:p.Ser810Pro
NM_153202.2:c.2350T>C NP_694882.1:p.Ser784Pro
XM_005260843.1:c.2467T>C XP_005260900.1:p.Ser823Pro
XM_006723639.1:c.2464T>C XP_006723702.1:p.Ser822Pro
XM_006723640.1:c.2458T>C XP_006723703.1:p.Ser820Pro
XM_011529366.1:c.2464T>C XP_011527668.1:p.Ser822Pro
XM_011529367.1:c.2425T>C XP_011527669.1:p.Ser809Pro
XM_011529368.1:c.2389T>C XP_011527670.1:p.Ser797Pro
XM_011529373.1:c.1465T>C XP_011527675.1:p.Ser489Pro
XR_937151.1:n.2479T>C
XR_937152.1:n.2476T>C
XR_937153.1:n.2449T>C
XR_937154.1:n.2449T>C
XR_937155.1:n.2370T>C
XR_937157.1:n.2372T>C
NM_001282447.2:c.2425T>C NP_001269376.1:p.Ser809Pro
NM_025220.4:c.2428T>C NP_079496.1:p.Ser810Pro
NM_153202.3:c.2350T>C NP_694882.1:p.Ser784Pro
XM_011529373.2:c.1465T>C XP_011527675.1:p.Ser489Pro
XR_001754405.1:n.2536T>C
XR_002958534.1:n.2645T>C
NM_001282447.3:c.2425T>C NP_001269376.1:p.Ser809Pro
NM_025220.5:c.2428T>C MANE Select NP_079496.1:p.Ser810Pro
NM_153202.4:c.2350T>C NP_694882.1:p.Ser784Pro