Canonical Allele Identifier: CA408103813
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669591G>T , CM000682.2:g.3669591G>T GRCh38
NC_000020.10:g.3650238G>T , CM000682.1:g.3650238G>T GRCh37
NC_000020.9:g.3598238G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2287C>A MANE Select ENSP00000348912.3:p.Pro763Thr
ENST00000350009.6:c.2209C>A ENSP00000322550.5:p.Pro737Thr
ENST00000356518.6:c.2287C>A ENSP00000348912.2:p.Pro763Thr
ENST00000379861.8:c.2287C>A ENSP00000369190.4:p.Pro763Thr
ENST00000466620.5:n.1848C>A
ENST00000483362.1:n.1035C>A
ENST00000617732.1:c.*974C>A ENSP00000483343.1:n.*974C>A
ENST00000619289.4:c.1927C>A ENSP00000484600.1:p.Pro643Thr
NM_001282447.1:c.2287C>A NP_001269376.1:p.Pro763Thr
NM_025220.3:c.2287C>A NP_079496.1:p.Pro763Thr
NM_153202.2:c.2209C>A NP_694882.1:p.Pro737Thr
XM_005260843.1:c.2326C>A XP_005260900.1:p.Pro776Thr
XM_006723639.1:c.2326C>A XP_006723702.1:p.Pro776Thr
XM_006723640.1:c.2317C>A XP_006723703.1:p.Pro773Thr
XM_011529366.1:c.2323C>A XP_011527668.1:p.Pro775Thr
XM_011529367.1:c.2284C>A XP_011527669.1:p.Pro762Thr
XM_011529368.1:c.2248C>A XP_011527670.1:p.Pro750Thr
XM_011529373.1:c.1324C>A XP_011527675.1:p.Pro442Thr
XR_937151.1:n.2384-221C>A
XR_937152.1:n.2384-221C>A
XR_937153.1:n.2311C>A
XR_937154.1:n.2311C>A
XR_937155.1:n.2232C>A
XR_937157.1:n.2234C>A
NM_001282447.2:c.2287C>A NP_001269376.1:p.Pro763Thr
NM_025220.4:c.2287C>A NP_079496.1:p.Pro763Thr
NM_153202.3:c.2209C>A NP_694882.1:p.Pro737Thr
XM_011529373.2:c.1324C>A XP_011527675.1:p.Pro442Thr
XR_001754405.1:n.2398C>A
XR_002958534.1:n.2507C>A
NM_001282447.3:c.2287C>A NP_001269376.1:p.Pro763Thr
NM_025220.5:c.2287C>A MANE Select NP_079496.1:p.Pro763Thr
NM_153202.4:c.2209C>A NP_694882.1:p.Pro737Thr