Canonical Allele Identifier: CA408103763

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650213G>C (hg19) ; chr20:g.3669566G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669566G>C , CM000682.2:g.3669566G>C	GRCh38
NC_000020.10:g.3650213G>C , CM000682.1:g.3650213G>C	GRCh37
NC_000020.9:g.3598213G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2312C>G MANE Select	ENSP00000348912.3:p.Thr771Ser
ENST00000350009.6:c.2234C>G	ENSP00000322550.5:p.Thr745Ser
ENST00000356518.6:c.2312C>G	ENSP00000348912.2:p.Thr771Ser
ENST00000379861.8:c.2312C>G	ENSP00000369190.4:p.Thr771Ser
ENST00000466620.5:n.1873C>G
ENST00000483362.1:n.1060C>G
ENST00000617732.1:c.*999C>G	ENSP00000483343.1:n.*999C>G
ENST00000619289.4:c.1952C>G	ENSP00000484600.1:p.Thr651Ser
NM_001282447.1:c.2312C>G	NP_001269376.1:p.Thr771Ser
NM_025220.3:c.2312C>G	NP_079496.1:p.Thr771Ser
NM_153202.2:c.2234C>G	NP_694882.1:p.Thr745Ser
XM_005260843.1:c.2351C>G	XP_005260900.1:p.Thr784Ser
XM_006723639.1:c.2351C>G	XP_006723702.1:p.Thr784Ser
XM_006723640.1:c.2342C>G	XP_006723703.1:p.Thr781Ser
XM_011529366.1:c.2348C>G	XP_011527668.1:p.Thr783Ser
XM_011529367.1:c.2309C>G	XP_011527669.1:p.Thr770Ser
XM_011529368.1:c.2273C>G	XP_011527670.1:p.Thr758Ser
XM_011529373.1:c.1349C>G	XP_011527675.1:p.Thr450Ser
XR_937151.1:n.2384-196C>G
XR_937152.1:n.2384-196C>G
XR_937153.1:n.2336C>G
XR_937154.1:n.2336C>G
XR_937155.1:n.2257C>G
XR_937157.1:n.2259C>G
NM_001282447.2:c.2312C>G	NP_001269376.1:p.Thr771Ser
NM_025220.4:c.2312C>G	NP_079496.1:p.Thr771Ser
NM_153202.3:c.2234C>G	NP_694882.1:p.Thr745Ser
XM_011529373.2:c.1349C>G	XP_011527675.1:p.Thr450Ser
XR_001754405.1:n.2423C>G
XR_002958534.1:n.2532C>G
NM_001282447.3:c.2312C>G	NP_001269376.1:p.Thr771Ser
NM_025220.5:c.2312C>G MANE Select	NP_079496.1:p.Thr771Ser
NM_153202.4:c.2234C>G	NP_694882.1:p.Thr745Ser