Canonical Allele Identifier: CA509560279

Gene: ADAM33

Linked Data

• dbSNP Id: rs1360618148
• gnomAD v2: 20-3654397-C-T
• gnomAD v4: 20-3673750-C-T
• MyVariant Identifiers: chr20:g.3654397C>T (hg19) ; chr20:g.3673750C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3673750C>T , CM000682.2:g.3673750C>T	GRCh38
NC_000020.10:g.3654397C>T , CM000682.1:g.3654397C>T	GRCh37
NC_000020.9:g.3602397C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.900G>A MANE Select	ENSP00000348912.3:p.Leu300=
ENST00000350009.6:c.900G>A	ENSP00000322550.5:p.Leu300=
ENST00000356518.6:c.900G>A	ENSP00000348912.2:p.Leu300=
ENST00000379861.8:c.900G>A	ENSP00000369190.4:p.Leu300=
ENST00000617732.1:c.*631+562G>A	ENSP00000483343.1:n.*631+562G>A
ENST00000619289.4:c.806+94G>A	ENSP00000484600.1:n.806+94G>A
NM_001282447.1:c.900G>A	NP_001269376.1:p.Leu300=
NM_025220.3:c.900G>A	NP_079496.1:p.Leu300=
NM_153202.2:c.900G>A	NP_694882.1:p.Leu300=
XM_005260843.1:c.939G>A	XP_005260900.1:p.Leu313=
XM_006723639.1:c.939G>A	XP_006723702.1:p.Leu313=
XM_006723640.1:c.939G>A	XP_006723703.1:p.Leu313=
XM_006723644.2:c.939G>A	XP_006723707.1:p.Leu313=
XM_011529366.1:c.936G>A	XP_011527668.1:p.Leu312=
XM_011529367.1:c.897G>A	XP_011527669.1:p.Leu299=
XM_011529368.1:c.939G>A	XP_011527670.1:p.Leu313=
XM_011529369.1:c.939G>A	XP_011527671.1:p.Leu313=
XM_011529370.1:c.939G>A	XP_011527672.1:p.Leu313=
XM_011529371.1:c.939G>A	XP_011527673.1:p.Leu313=
XM_011529372.1:c.939G>A	XP_011527674.1:p.Leu313=
XM_011529373.1:c.-141G>A	XP_011527675.1:n.-141G>A
XR_937151.1:n.1043G>A
XR_937152.1:n.1043G>A
XR_937153.1:n.1043G>A
XR_937154.1:n.1043G>A
XR_937155.1:n.964G>A
XR_937157.1:n.1043G>A
NM_001282447.2:c.900G>A	NP_001269376.1:p.Leu300=
NM_025220.4:c.900G>A	NP_079496.1:p.Leu300=
NM_153202.3:c.900G>A	NP_694882.1:p.Leu300=
XM_011529371.2:c.939G>A	XP_011527673.1:p.Leu313=
XM_011529373.2:c.-141G>A	XP_011527675.1:n.-141G>A
XM_017028080.2:c.939G>A	XP_016883569.1:p.Leu313=
XM_017028081.2:c.900G>A	XP_016883570.1:p.Leu300=
XM_017028082.1:c.939G>A	XP_016883571.1:p.Leu313=
XM_017028083.1:c.939G>A	XP_016883572.1:p.Leu313=
XR_001754405.1:n.1043G>A
XR_002958534.1:n.1043G>A
NM_001282447.3:c.900G>A	NP_001269376.1:p.Leu300=
NM_025220.5:c.900G>A MANE Select	NP_079496.1:p.Leu300=
NM_153202.4:c.900G>A	NP_694882.1:p.Leu300=