Canonical Allele Identifier: CA9745541

Gene: ADAM33

Linked Data

• dbSNP Id: rs749970775
• ExAC: 20:3654384 G / A
• gnomAD v2: 20-3654384-G-A
• gnomAD v4: 20-3673737-G-A
• MyVariant Identifiers: chr20:g.3654384G>A (hg19) ; chr20:g.3673737G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3673737G>A , CM000682.2:g.3673737G>A	GRCh38
NC_000020.10:g.3654384G>A , CM000682.1:g.3654384G>A	GRCh37
NC_000020.9:g.3602384G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.905+8C>T MANE Select	ENSP00000348912.3:n.905+8C>T
ENST00000350009.6:c.905+8C>T	ENSP00000322550.5:n.905+8C>T
ENST00000356518.6:c.905+8C>T	ENSP00000348912.2:n.905+8C>T
ENST00000379861.8:c.905+8C>T	ENSP00000369190.4:n.905+8C>T
ENST00000466620.5:n.11C>T
ENST00000617732.1:c.*631+575C>T	ENSP00000483343.1:n.*631+575C>T
ENST00000619289.4:c.806+107C>T	ENSP00000484600.1:n.806+107C>T
NM_001282447.1:c.905+8C>T	NP_001269376.1:n.905+8C>T
NM_025220.3:c.905+8C>T	NP_079496.1:n.905+8C>T
NM_153202.2:c.905+8C>T	NP_694882.1:n.905+8C>T
XM_005260843.1:c.944+8C>T	XP_005260900.1:n.944+8C>T
XM_006723639.1:c.944+8C>T	XP_006723702.1:n.944+8C>T
XM_006723640.1:c.944+8C>T	XP_006723703.1:n.944+8C>T
XM_006723644.2:c.944+8C>T	XP_006723707.1:n.944+8C>T
XM_011529366.1:c.941+8C>T	XP_011527668.1:n.941+8C>T
XM_011529367.1:c.902+8C>T	XP_011527669.1:n.902+8C>T
XM_011529368.1:c.944+8C>T	XP_011527670.1:n.944+8C>T
XM_011529369.1:c.944+8C>T	XP_011527671.1:n.944+8C>T
XM_011529370.1:c.944+8C>T	XP_011527672.1:n.944+8C>T
XM_011529371.1:c.944+8C>T	XP_011527673.1:n.944+8C>T
XM_011529372.1:c.944+8C>T	XP_011527674.1:n.944+8C>T
XM_011529373.1:c.-128C>T	XP_011527675.1:n.-128C>T
XR_937151.1:n.1048+8C>T
XR_937152.1:n.1048+8C>T
XR_937153.1:n.1048+8C>T
XR_937154.1:n.1056C>T
XR_937155.1:n.977C>T
XR_937157.1:n.1048+8C>T
NM_001282447.2:c.905+8C>T	NP_001269376.1:n.905+8C>T
NM_025220.4:c.905+8C>T	NP_079496.1:n.905+8C>T
NM_153202.3:c.905+8C>T	NP_694882.1:n.905+8C>T
XM_011529371.2:c.944+8C>T	XP_011527673.1:n.944+8C>T
XM_011529373.2:c.-128C>T	XP_011527675.1:n.-128C>T
XM_017028080.2:c.952C>T	XP_016883569.1:p.Pro318Ser
XM_017028081.2:c.913C>T	XP_016883570.1:p.Pro305Ser
XM_017028082.1:c.944+8C>T	XP_016883571.1:n.944+8C>T
XM_017028083.1:c.944+8C>T	XP_016883572.1:n.944+8C>T
XR_001754405.1:n.1048+8C>T
XR_002958534.1:n.1048+8C>T
NM_001282447.3:c.905+8C>T	NP_001269376.1:n.905+8C>T
NM_025220.5:c.905+8C>T MANE Select	NP_079496.1:n.905+8C>T
NM_153202.4:c.905+8C>T	NP_694882.1:n.905+8C>T