Canonical Allele Identifier: CA744017506

Gene: ADAM33

Linked Data

• dbSNP Id: rs1181216467
• gnomAD v4: 20-3673686-C-A
• MyVariant Identifiers: chr20:g.3654333C>A (hg19) ; chr20:g.3673686C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3673686C>A , CM000682.2:g.3673686C>A	GRCh38
NC_000020.10:g.3654333C>A , CM000682.1:g.3654333C>A	GRCh37
NC_000020.9:g.3602333C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.906-28G>T MANE Select	ENSP00000348912.3:n.906-28G>T
ENST00000350009.6:c.906-28G>T	ENSP00000322550.5:n.906-28G>T
ENST00000356518.6:c.906-28G>T	ENSP00000348912.2:n.906-28G>T
ENST00000379861.8:c.906-28G>T	ENSP00000369190.4:n.906-28G>T
ENST00000466620.5:n.62G>T
ENST00000617732.1:c.*631+626G>T	ENSP00000483343.1:n.*631+626G>T
ENST00000619289.4:c.806+158G>T	ENSP00000484600.1:n.806+158G>T
NM_001282447.1:c.906-28G>T	NP_001269376.1:n.906-28G>T
NM_025220.3:c.906-28G>T	NP_079496.1:n.906-28G>T
NM_153202.2:c.906-28G>T	NP_694882.1:n.906-28G>T
XM_005260843.1:c.945-28G>T	XP_005260900.1:n.945-28G>T
XM_006723639.1:c.945-28G>T	XP_006723702.1:n.945-28G>T
XM_006723640.1:c.945-28G>T	XP_006723703.1:n.945-28G>T
XM_006723644.2:c.945-28G>T	XP_006723707.1:n.945-28G>T
XM_011529366.1:c.942-28G>T	XP_011527668.1:n.942-28G>T
XM_011529367.1:c.903-28G>T	XP_011527669.1:n.903-28G>T
XM_011529368.1:c.945-28G>T	XP_011527670.1:n.945-28G>T
XM_011529369.1:c.945-28G>T	XP_011527671.1:n.945-28G>T
XM_011529370.1:c.945-28G>T	XP_011527672.1:n.945-28G>T
XM_011529371.1:c.945-28G>T	XP_011527673.1:n.945-28G>T
XM_011529372.1:c.945-28G>T	XP_011527674.1:n.945-28G>T
XM_011529373.1:c.-77G>T	XP_011527675.1:n.-77G>T
XR_937151.1:n.1049-28G>T
XR_937152.1:n.1049-28G>T
XR_937153.1:n.1049-28G>T
XR_937154.1:n.1107G>T
XR_937155.1:n.1028G>T
XR_937157.1:n.1049-28G>T
NM_001282447.2:c.906-28G>T	NP_001269376.1:n.906-28G>T
NM_025220.4:c.906-28G>T	NP_079496.1:n.906-28G>T
NM_153202.3:c.906-28G>T	NP_694882.1:n.906-28G>T
XM_011529371.2:c.945-28G>T	XP_011527673.1:n.945-28G>T
XM_011529373.2:c.-77G>T	XP_011527675.1:n.-77G>T
XM_017028080.2:c.1003G>T	XP_016883569.1:p.Ala335Ser
XM_017028081.2:c.964G>T	XP_016883570.1:p.Ala322Ser
XM_017028082.1:c.945-28G>T	XP_016883571.1:n.945-28G>T
XM_017028083.1:c.945-28G>T	XP_016883572.1:n.945-28G>T
XR_001754405.1:n.1049-28G>T
XR_002958534.1:n.1049-28G>T
NM_001282447.3:c.906-28G>T	NP_001269376.1:n.906-28G>T
NM_025220.5:c.906-28G>T MANE Select	NP_079496.1:n.906-28G>T
NM_153202.4:c.906-28G>T	NP_694882.1:n.906-28G>T