Canonical Allele Identifier: CA408103750

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3669561-G-A
• MyVariant Identifiers: chr20:g.3650208G>A (hg19) ; chr20:g.3669561G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669561G>A , CM000682.2:g.3669561G>A	GRCh38
NC_000020.10:g.3650208G>A , CM000682.1:g.3650208G>A	GRCh37
NC_000020.9:g.3598208G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2317C>T MANE Select	ENSP00000348912.3:p.Gln773Ter
ENST00000350009.6:c.2239C>T	ENSP00000322550.5:p.Gln747Ter
ENST00000356518.6:c.2317C>T	ENSP00000348912.2:p.Gln773Ter
ENST00000379861.8:c.2317C>T	ENSP00000369190.4:p.Gln773Ter
ENST00000466620.5:n.1878C>T
ENST00000483362.1:n.1065C>T
ENST00000617732.1:c.*1004C>T	ENSP00000483343.1:n.*1004C>T
ENST00000619289.4:c.1957C>T	ENSP00000484600.1:p.Gln653Ter
NM_001282447.1:c.2317C>T	NP_001269376.1:p.Gln773Ter
NM_025220.3:c.2317C>T	NP_079496.1:p.Gln773Ter
NM_153202.2:c.2239C>T	NP_694882.1:p.Gln747Ter
XM_005260843.1:c.2356C>T	XP_005260900.1:p.Gln786Ter
XM_006723639.1:c.2356C>T	XP_006723702.1:p.Gln786Ter
XM_006723640.1:c.2347C>T	XP_006723703.1:p.Gln783Ter
XM_011529366.1:c.2353C>T	XP_011527668.1:p.Gln785Ter
XM_011529367.1:c.2314C>T	XP_011527669.1:p.Gln772Ter
XM_011529368.1:c.2278C>T	XP_011527670.1:p.Gln760Ter
XM_011529373.1:c.1354C>T	XP_011527675.1:p.Gln452Ter
XR_937151.1:n.2384-191C>T
XR_937152.1:n.2384-191C>T
XR_937153.1:n.2341C>T
XR_937154.1:n.2341C>T
XR_937155.1:n.2262C>T
XR_937157.1:n.2264C>T
NM_001282447.2:c.2317C>T	NP_001269376.1:p.Gln773Ter
NM_025220.4:c.2317C>T	NP_079496.1:p.Gln773Ter
NM_153202.3:c.2239C>T	NP_694882.1:p.Gln747Ter
XM_011529373.2:c.1354C>T	XP_011527675.1:p.Gln452Ter
XR_001754405.1:n.2428C>T
XR_002958534.1:n.2537C>T
NM_001282447.3:c.2317C>T	NP_001269376.1:p.Gln773Ter
NM_025220.5:c.2317C>T MANE Select	NP_079496.1:p.Gln773Ter
NM_153202.4:c.2239C>T	NP_694882.1:p.Gln747Ter