Canonical Allele Identifier: CA408103447
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668985A>T , CM000682.2:g.3668985A>T GRCh38
NC_000020.10:g.3649632A>T , CM000682.1:g.3649632A>T GRCh37
NC_000020.9:g.3597632A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2420T>A MANE Select ENSP00000348912.3:p.Met807Lys
ENST00000350009.6:c.2342T>A ENSP00000322550.5:p.Met781Lys
ENST00000356518.6:c.2420T>A ENSP00000348912.2:p.Met807Lys
ENST00000379861.8:c.2417T>A ENSP00000369190.4:p.Met806Lys
ENST00000466620.5:n.1981T>A
ENST00000483362.1:n.1343T>A
ENST00000617732.1:c.*1104T>A ENSP00000483343.1:n.*1104T>A
ENST00000619289.4:c.2057T>A ENSP00000484600.1:p.Met686Lys
NM_001282447.1:c.2417T>A NP_001269376.1:p.Met806Lys
NM_025220.3:c.2420T>A NP_079496.1:p.Met807Lys
NM_153202.2:c.2342T>A NP_694882.1:p.Met781Lys
XM_005260843.1:c.2459T>A XP_005260900.1:p.Met820Lys
XM_006723639.1:c.2456T>A XP_006723702.1:p.Met819Lys
XM_006723640.1:c.2450T>A XP_006723703.1:p.Met817Lys
XM_011529366.1:c.2456T>A XP_011527668.1:p.Met819Lys
XM_011529367.1:c.2417T>A XP_011527669.1:p.Met806Lys
XM_011529368.1:c.2381T>A XP_011527670.1:p.Met794Lys
XM_011529373.1:c.1457T>A XP_011527675.1:p.Met486Lys
XR_937151.1:n.2471T>A
XR_937152.1:n.2468T>A
XR_937153.1:n.2441T>A
XR_937154.1:n.2441T>A
XR_937155.1:n.2362T>A
XR_937157.1:n.2364T>A
NM_001282447.2:c.2417T>A NP_001269376.1:p.Met806Lys
NM_025220.4:c.2420T>A NP_079496.1:p.Met807Lys
NM_153202.3:c.2342T>A NP_694882.1:p.Met781Lys
XM_011529373.2:c.1457T>A XP_011527675.1:p.Met486Lys
XR_001754405.1:n.2528T>A
XR_002958534.1:n.2637T>A
NM_001282447.3:c.2417T>A NP_001269376.1:p.Met806Lys
NM_025220.5:c.2420T>A MANE Select NP_079496.1:p.Met807Lys
NM_153202.4:c.2342T>A NP_694882.1:p.Met781Lys