Canonical Allele Identifier: CA408103742

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650205G>T (hg19) ; chr20:g.3669558G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669558G>T , CM000682.2:g.3669558G>T	GRCh38
NC_000020.10:g.3650205G>T , CM000682.1:g.3650205G>T	GRCh37
NC_000020.9:g.3598205G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2320C>A MANE Select	ENSP00000348912.3:p.Pro774Thr
ENST00000350009.6:c.2242C>A	ENSP00000322550.5:p.Pro748Thr
ENST00000356518.6:c.2320C>A	ENSP00000348912.2:p.Pro774Thr
ENST00000379861.8:c.2320C>A	ENSP00000369190.4:p.Pro774Thr
ENST00000466620.5:n.1881C>A
ENST00000483362.1:n.1068C>A
ENST00000617732.1:c.*1007C>A	ENSP00000483343.1:n.*1007C>A
ENST00000619289.4:c.1960C>A	ENSP00000484600.1:p.Pro654Thr
NM_001282447.1:c.2320C>A	NP_001269376.1:p.Pro774Thr
NM_025220.3:c.2320C>A	NP_079496.1:p.Pro774Thr
NM_153202.2:c.2242C>A	NP_694882.1:p.Pro748Thr
XM_005260843.1:c.2359C>A	XP_005260900.1:p.Pro787Thr
XM_006723639.1:c.2359C>A	XP_006723702.1:p.Pro787Thr
XM_006723640.1:c.2350C>A	XP_006723703.1:p.Pro784Thr
XM_011529366.1:c.2356C>A	XP_011527668.1:p.Pro786Thr
XM_011529367.1:c.2317C>A	XP_011527669.1:p.Pro773Thr
XM_011529368.1:c.2281C>A	XP_011527670.1:p.Pro761Thr
XM_011529373.1:c.1357C>A	XP_011527675.1:p.Pro453Thr
XR_937151.1:n.2384-188C>A
XR_937152.1:n.2384-188C>A
XR_937153.1:n.2344C>A
XR_937154.1:n.2344C>A
XR_937155.1:n.2265C>A
XR_937157.1:n.2267C>A
NM_001282447.2:c.2320C>A	NP_001269376.1:p.Pro774Thr
NM_025220.4:c.2320C>A	NP_079496.1:p.Pro774Thr
NM_153202.3:c.2242C>A	NP_694882.1:p.Pro748Thr
XM_011529373.2:c.1357C>A	XP_011527675.1:p.Pro453Thr
XR_001754405.1:n.2431C>A
XR_002958534.1:n.2540C>A
NM_001282447.3:c.2320C>A	NP_001269376.1:p.Pro774Thr
NM_025220.5:c.2320C>A MANE Select	NP_079496.1:p.Pro774Thr
NM_153202.4:c.2242C>A	NP_694882.1:p.Pro748Thr