Canonical Allele Identifier: CA9745555
Gene: ADAM33 HGNC NCBI

Linked Data

dbSNP Id: rs41534847

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3673835G>A , CM000682.2:g.3673835G>A GRCh38
NC_000020.10:g.3654482G>A , CM000682.1:g.3654482G>A GRCh37
NC_000020.9:g.3602482G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.815C>T MANE Select ENSP00000348912.3:p.Thr272Met
ENST00000350009.6:c.815C>T ENSP00000322550.5:p.Thr272Met
ENST00000356518.6:c.815C>T ENSP00000348912.2:p.Thr272Met
ENST00000379861.8:c.815C>T ENSP00000369190.4:p.Thr272Met
ENST00000617732.1:c.*631+477C>T ENSP00000483343.1:n.*631+477C>T
ENST00000619289.4:c.806+9C>T ENSP00000484600.1:n.806+9C>T
NM_001282447.1:c.815C>T NP_001269376.1:p.Thr272Met
NM_025220.3:c.815C>T NP_079496.1:p.Thr272Met
NM_153202.2:c.815C>T NP_694882.1:p.Thr272Met
XM_005260843.1:c.854C>T XP_005260900.1:p.Thr285Met
XM_006723639.1:c.854C>T XP_006723702.1:p.Thr285Met
XM_006723640.1:c.854C>T XP_006723703.1:p.Thr285Met
XM_006723644.2:c.854C>T XP_006723707.1:p.Thr285Met
XM_011529366.1:c.851C>T XP_011527668.1:p.Thr284Met
XM_011529367.1:c.812C>T XP_011527669.1:p.Thr271Met
XM_011529368.1:c.854C>T XP_011527670.1:p.Thr285Met
XM_011529369.1:c.854C>T XP_011527671.1:p.Thr285Met
XM_011529370.1:c.854C>T XP_011527672.1:p.Thr285Met
XM_011529371.1:c.854C>T XP_011527673.1:p.Thr285Met
XM_011529372.1:c.854C>T XP_011527674.1:p.Thr285Met
XM_011529373.1:c.-226C>T XP_011527675.1:n.-226C>T
XR_937151.1:n.958C>T
XR_937152.1:n.958C>T
XR_937153.1:n.958C>T
XR_937154.1:n.958C>T
XR_937155.1:n.879C>T
XR_937157.1:n.958C>T
NM_001282447.2:c.815C>T NP_001269376.1:p.Thr272Met
NM_025220.4:c.815C>T NP_079496.1:p.Thr272Met
NM_153202.3:c.815C>T NP_694882.1:p.Thr272Met
XM_011529371.2:c.854C>T XP_011527673.1:p.Thr285Met
XM_011529373.2:c.-226C>T XP_011527675.1:n.-226C>T
XM_017028080.2:c.854C>T XP_016883569.1:p.Thr285Met
XM_017028081.2:c.815C>T XP_016883570.1:p.Thr272Met
XM_017028082.1:c.854C>T XP_016883571.1:p.Thr285Met
XM_017028083.1:c.854C>T XP_016883572.1:p.Thr285Met
XR_001754405.1:n.958C>T
XR_002958534.1:n.958C>T
NM_001282447.3:c.815C>T NP_001269376.1:p.Thr272Met
NM_025220.5:c.815C>T MANE Select NP_079496.1:p.Thr272Met
NM_153202.4:c.815C>T NP_694882.1:p.Thr272Met