Canonical Allele Identifier: CA310997378

Gene: ADAM33

Linked Data

• dbSNP Id: rs553889164
• gnomAD v3: 20-3668607-A-G
• gnomAD v4: 20-3668607-A-G
• MyVariant Identifiers: chr20:g.3649254A>G (hg19) ; chr20:g.3668607A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668607A>G , CM000682.2:g.3668607A>G	GRCh38
NC_000020.10:g.3649254A>G , CM000682.1:g.3649254A>G	GRCh37
NC_000020.9:g.3597254A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.*356T>C MANE Select	ENSP00000348912.3:n.*356T>C
ENST00000350009.6:c.*356T>C	ENSP00000322550.5:n.*356T>C
ENST00000356518.6:c.*356T>C	ENSP00000348912.2:n.*356T>C
ENST00000379861.8:c.*356T>C	ENSP00000369190.4:n.*356T>C
ENST00000466620.5:n.2359T>C
ENST00000483362.1:n.1721T>C
ENST00000617732.1:c.*1482T>C	ENSP00000483343.1:n.*1482T>C
ENST00000619289.4:c.*356T>C	ENSP00000484600.1:n.*356T>C
NM_001282447.1:c.*356T>C	NP_001269376.1:n.*356T>C
NM_025220.3:c.*356T>C	NP_079496.1:n.*356T>C
NM_153202.2:c.*356T>C	NP_694882.1:n.*356T>C
XM_005260843.1:c.*356T>C	XP_005260900.1:n.*356T>C
XM_006723639.1:c.*356T>C	XP_006723702.1:n.*356T>C
XM_006723640.1:c.*356T>C	XP_006723703.1:n.*356T>C
XM_011529366.1:c.*356T>C	XP_011527668.1:n.*356T>C
XM_011529367.1:c.*356T>C	XP_011527669.1:n.*356T>C
XM_011529368.1:c.*356T>C	XP_011527670.1:n.*356T>C
XM_011529373.1:c.*356T>C	XP_011527675.1:n.*356T>C
XR_937153.1:n.2819T>C
XR_937154.1:n.2819T>C
XR_937155.1:n.2740T>C
XR_937157.1:n.2742T>C
NM_001282447.2:c.*356T>C	NP_001269376.1:n.*356T>C
NM_025220.4:c.*356T>C	NP_079496.1:n.*356T>C
NM_153202.3:c.*356T>C	NP_694882.1:n.*356T>C
XM_011529373.2:c.*356T>C	XP_011527675.1:n.*356T>C
XR_001754405.1:n.2906T>C
XR_002958534.1:n.3015T>C
NM_001282447.3:c.*356T>C	NP_001269376.1:n.*356T>C
NM_025220.5:c.*356T>C MANE Select	NP_079496.1:n.*356T>C
NM_153202.4:c.*356T>C	NP_694882.1:n.*356T>C