Canonical Allele Identifier: CA408103651

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650008T>G (hg19) ; chr20:g.3669361T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669361T>G , CM000682.2:g.3669361T>G	GRCh38
NC_000020.10:g.3650008T>G , CM000682.1:g.3650008T>G	GRCh37
NC_000020.9:g.3598008T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2342A>C MANE Select	ENSP00000348912.3:p.Asn781Thr
ENST00000350009.6:c.2264A>C	ENSP00000322550.5:p.Asn755Thr
ENST00000356518.6:c.2342A>C	ENSP00000348912.2:p.Asn781Thr
ENST00000379861.8:c.2342A>C	ENSP00000369190.4:p.Asn781Thr
ENST00000466620.5:n.1903A>C
ENST00000483362.1:n.1265A>C
ENST00000617732.1:c.*1029A>C	ENSP00000483343.1:n.*1029A>C
ENST00000619289.4:c.1982A>C	ENSP00000484600.1:p.Asn661Thr
NM_001282447.1:c.2342A>C	NP_001269376.1:p.Asn781Thr
NM_025220.3:c.2342A>C	NP_079496.1:p.Asn781Thr
NM_153202.2:c.2264A>C	NP_694882.1:p.Asn755Thr
XM_005260843.1:c.2381A>C	XP_005260900.1:p.Asn794Thr
XM_006723639.1:c.2381A>C	XP_006723702.1:p.Asn794Thr
XM_006723640.1:c.2372A>C	XP_006723703.1:p.Asn791Thr
XM_011529366.1:c.2378A>C	XP_011527668.1:p.Asn793Thr
XM_011529367.1:c.2339A>C	XP_011527669.1:p.Asn780Thr
XM_011529368.1:c.2303A>C	XP_011527670.1:p.Asn768Thr
XM_011529373.1:c.1379A>C	XP_011527675.1:p.Asn460Thr
XR_937151.1:n.2393A>C
XR_937152.1:n.2393A>C
XR_937153.1:n.2366A>C
XR_937154.1:n.2366A>C
XR_937155.1:n.2287A>C
XR_937157.1:n.2289A>C
NM_001282447.2:c.2342A>C	NP_001269376.1:p.Asn781Thr
NM_025220.4:c.2342A>C	NP_079496.1:p.Asn781Thr
NM_153202.3:c.2264A>C	NP_694882.1:p.Asn755Thr
XM_011529373.2:c.1379A>C	XP_011527675.1:p.Asn460Thr
XR_001754405.1:n.2453A>C
XR_002958534.1:n.2562A>C
NM_001282447.3:c.2342A>C	NP_001269376.1:p.Asn781Thr
NM_025220.5:c.2342A>C MANE Select	NP_079496.1:p.Asn781Thr
NM_153202.4:c.2264A>C	NP_694882.1:p.Asn755Thr