Canonical Allele Identifier: CA509419240

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650218T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669571T>A , CM000682.2:g.3669571T>A	GRCh38
NC_000020.10:g.3650218T>A , CM000682.1:g.3650218T>A	GRCh37
NC_000020.9:g.3598218T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2307A>T MANE Select	ENSP00000348912.3:p.Thr769=
ENST00000350009.6:c.2229A>T	ENSP00000322550.5:p.Thr743=
ENST00000356518.6:c.2307A>T	ENSP00000348912.2:p.Thr769=
ENST00000379861.8:c.2307A>T	ENSP00000369190.4:p.Thr769=
ENST00000466620.5:n.1868A>T
ENST00000483362.1:n.1055A>T
ENST00000617732.1:c.*994A>T	ENSP00000483343.1:n.*994A>T
ENST00000619289.4:c.1947A>T	ENSP00000484600.1:p.Thr649=
NM_001282447.1:c.2307A>T	NP_001269376.1:p.Thr769=
NM_025220.3:c.2307A>T	NP_079496.1:p.Thr769=
NM_153202.2:c.2229A>T	NP_694882.1:p.Thr743=
XM_005260843.1:c.2346A>T	XP_005260900.1:p.Thr782=
XM_006723639.1:c.2346A>T	XP_006723702.1:p.Thr782=
XM_006723640.1:c.2337A>T	XP_006723703.1:p.Thr779=
XM_011529366.1:c.2343A>T	XP_011527668.1:p.Thr781=
XM_011529367.1:c.2304A>T	XP_011527669.1:p.Thr768=
XM_011529368.1:c.2268A>T	XP_011527670.1:p.Thr756=
XM_011529373.1:c.1344A>T	XP_011527675.1:p.Thr448=
XR_937151.1:n.2384-201A>T
XR_937152.1:n.2384-201A>T
XR_937153.1:n.2331A>T
XR_937154.1:n.2331A>T
XR_937155.1:n.2252A>T
XR_937157.1:n.2254A>T
NM_001282447.2:c.2307A>T	NP_001269376.1:p.Thr769=
NM_025220.4:c.2307A>T	NP_079496.1:p.Thr769=
NM_153202.3:c.2229A>T	NP_694882.1:p.Thr743=
XM_011529373.2:c.1344A>T	XP_011527675.1:p.Thr448=
XR_001754405.1:n.2418A>T
XR_002958534.1:n.2527A>T
NM_001282447.3:c.2307A>T	NP_001269376.1:p.Thr769=
NM_025220.5:c.2307A>T MANE Select	NP_079496.1:p.Thr769=
NM_153202.4:c.2229A>T	NP_694882.1:p.Thr743=