Canonical Allele Identifier: CA310997363

Gene: ADAM33

Linked Data

• dbSNP Id: rs1004092306
• gnomAD v2: 20-3649228-C-A
• gnomAD v3: 20-3668581-C-A
• gnomAD v4: 20-3668581-C-A
• MyVariant Identifiers: chr20:g.3649228C>A (hg19) ; chr20:g.3668581C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668581C>A , CM000682.2:g.3668581C>A	GRCh38
NC_000020.10:g.3649228C>A , CM000682.1:g.3649228C>A	GRCh37
NC_000020.9:g.3597228C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.*382G>T MANE Select	ENSP00000348912.3:n.*382G>T
ENST00000350009.6:c.*382G>T	ENSP00000322550.5:n.*382G>T
ENST00000356518.6:c.*382G>T	ENSP00000348912.2:n.*382G>T
ENST00000379861.8:c.*382G>T	ENSP00000369190.4:n.*382G>T
ENST00000466620.5:n.2385G>T
ENST00000483362.1:n.1747G>T
ENST00000619289.4:c.*382G>T	ENSP00000484600.1:n.*382G>T
NM_001282447.1:c.*382G>T	NP_001269376.1:n.*382G>T
NM_025220.3:c.*382G>T	NP_079496.1:n.*382G>T
NM_153202.2:c.*382G>T	NP_694882.1:n.*382G>T
XM_005260843.1:c.*382G>T	XP_005260900.1:n.*382G>T
XM_006723639.1:c.*382G>T	XP_006723702.1:n.*382G>T
XM_006723640.1:c.*382G>T	XP_006723703.1:n.*382G>T
XM_011529366.1:c.*382G>T	XP_011527668.1:n.*382G>T
XM_011529367.1:c.*382G>T	XP_011527669.1:n.*382G>T
XM_011529368.1:c.*382G>T	XP_011527670.1:n.*382G>T
XM_011529373.1:c.*382G>T	XP_011527675.1:n.*382G>T
XR_937153.1:n.2845G>T
XR_937154.1:n.2845G>T
XR_937155.1:n.2766G>T
XR_937157.1:n.2768G>T
NM_001282447.2:c.*382G>T	NP_001269376.1:n.*382G>T
NM_025220.4:c.*382G>T	NP_079496.1:n.*382G>T
NM_153202.3:c.*382G>T	NP_694882.1:n.*382G>T
XM_011529373.2:c.*382G>T	XP_011527675.1:n.*382G>T
XR_001754405.1:n.2932G>T
XR_002958534.1:n.3041G>T
NM_001282447.3:c.*382G>T	NP_001269376.1:n.*382G>T
NM_025220.5:c.*382G>T MANE Select	NP_079496.1:n.*382G>T
NM_153202.4:c.*382G>T	NP_694882.1:n.*382G>T