Canonical Allele Identifier: CA408103540

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649969G>C (hg19) ; chr20:g.3669322G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669322G>C , CM000682.2:g.3669322G>C	GRCh38
NC_000020.10:g.3649969G>C , CM000682.1:g.3649969G>C	GRCh37
NC_000020.9:g.3597969G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2381C>G MANE Select	ENSP00000348912.3:p.Pro794Arg
ENST00000350009.6:c.2303C>G	ENSP00000322550.5:p.Pro768Arg
ENST00000356518.6:c.2381C>G	ENSP00000348912.2:p.Pro794Arg
ENST00000379861.8:c.2381C>G	ENSP00000369190.4:p.Pro794Arg
ENST00000466620.5:n.1942C>G
ENST00000483362.1:n.1304C>G
ENST00000617732.1:c.*1068C>G	ENSP00000483343.1:n.*1068C>G
ENST00000619289.4:c.2021C>G	ENSP00000484600.1:p.Pro674Arg
NM_001282447.1:c.2381C>G	NP_001269376.1:p.Pro794Arg
NM_025220.3:c.2381C>G	NP_079496.1:p.Pro794Arg
NM_153202.2:c.2303C>G	NP_694882.1:p.Pro768Arg
XM_005260843.1:c.2420C>G	XP_005260900.1:p.Pro807Arg
XM_006723639.1:c.2420C>G	XP_006723702.1:p.Pro807Arg
XM_006723640.1:c.2411C>G	XP_006723703.1:p.Pro804Arg
XM_011529366.1:c.2417C>G	XP_011527668.1:p.Pro806Arg
XM_011529367.1:c.2378C>G	XP_011527669.1:p.Pro793Arg
XM_011529368.1:c.2342C>G	XP_011527670.1:p.Pro781Arg
XM_011529373.1:c.1418C>G	XP_011527675.1:p.Pro473Arg
XR_937151.1:n.2432C>G
XR_937152.1:n.2432C>G
XR_937153.1:n.2405C>G
XR_937154.1:n.2405C>G
XR_937155.1:n.2326C>G
XR_937157.1:n.2328C>G
NM_001282447.2:c.2381C>G	NP_001269376.1:p.Pro794Arg
NM_025220.4:c.2381C>G	NP_079496.1:p.Pro794Arg
NM_153202.3:c.2303C>G	NP_694882.1:p.Pro768Arg
XM_011529373.2:c.1418C>G	XP_011527675.1:p.Pro473Arg
XR_001754405.1:n.2492C>G
XR_002958534.1:n.2601C>G
NM_001282447.3:c.2381C>G	NP_001269376.1:p.Pro794Arg
NM_025220.5:c.2381C>G MANE Select	NP_079496.1:p.Pro794Arg
NM_153202.4:c.2303C>G	NP_694882.1:p.Pro768Arg