Canonical Allele Identifier: CA408103776

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3669573-T-C
• MyVariant Identifiers: chr20:g.3650220T>C (hg19) ; chr20:g.3669573T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669573T>C , CM000682.2:g.3669573T>C	GRCh38
NC_000020.10:g.3650220T>C , CM000682.1:g.3650220T>C	GRCh37
NC_000020.9:g.3598220T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2305A>G MANE Select	ENSP00000348912.3:p.Thr769Ala
ENST00000350009.6:c.2227A>G	ENSP00000322550.5:p.Thr743Ala
ENST00000356518.6:c.2305A>G	ENSP00000348912.2:p.Thr769Ala
ENST00000379861.8:c.2305A>G	ENSP00000369190.4:p.Thr769Ala
ENST00000466620.5:n.1866A>G
ENST00000483362.1:n.1053A>G
ENST00000617732.1:c.*992A>G	ENSP00000483343.1:n.*992A>G
ENST00000619289.4:c.1945A>G	ENSP00000484600.1:p.Thr649Ala
NM_001282447.1:c.2305A>G	NP_001269376.1:p.Thr769Ala
NM_025220.3:c.2305A>G	NP_079496.1:p.Thr769Ala
NM_153202.2:c.2227A>G	NP_694882.1:p.Thr743Ala
XM_005260843.1:c.2344A>G	XP_005260900.1:p.Thr782Ala
XM_006723639.1:c.2344A>G	XP_006723702.1:p.Thr782Ala
XM_006723640.1:c.2335A>G	XP_006723703.1:p.Thr779Ala
XM_011529366.1:c.2341A>G	XP_011527668.1:p.Thr781Ala
XM_011529367.1:c.2302A>G	XP_011527669.1:p.Thr768Ala
XM_011529368.1:c.2266A>G	XP_011527670.1:p.Thr756Ala
XM_011529373.1:c.1342A>G	XP_011527675.1:p.Thr448Ala
XR_937151.1:n.2384-203A>G
XR_937152.1:n.2384-203A>G
XR_937153.1:n.2329A>G
XR_937154.1:n.2329A>G
XR_937155.1:n.2250A>G
XR_937157.1:n.2252A>G
NM_001282447.2:c.2305A>G	NP_001269376.1:p.Thr769Ala
NM_025220.4:c.2305A>G	NP_079496.1:p.Thr769Ala
NM_153202.3:c.2227A>G	NP_694882.1:p.Thr743Ala
XM_011529373.2:c.1342A>G	XP_011527675.1:p.Thr448Ala
XR_001754405.1:n.2416A>G
XR_002958534.1:n.2525A>G
NM_001282447.3:c.2305A>G	NP_001269376.1:p.Thr769Ala
NM_025220.5:c.2305A>G MANE Select	NP_079496.1:p.Thr769Ala
NM_153202.4:c.2227A>G	NP_694882.1:p.Thr743Ala