Canonical Allele Identifier: CA2651722832

Gene: ADAM33

Linked Data

• gnomAD v4: 20-3668462-A-ATCT

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668462_3668463insTCT , CM000682.2:g.3668462_3668463insTCT	GRCh38
NC_000020.10:g.3649109_3649110insTCT , CM000682.1:g.3649109_3649110insTCT	GRCh37
NC_000020.9:g.3597109_3597110insTCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.*500_*501insAGA MANE Select	ENSP00000348912.3:n.*500_*501insAGA
ENST00000350009.6:c.*500_*501insAGA	ENSP00000322550.5:n.*500_*501insAGA
ENST00000356518.6:c.*500_*501insAGA	ENSP00000348912.2:n.*500_*501insAGA
ENST00000379861.8:c.*500_*501insAGA	ENSP00000369190.4:n.*500_*501insAGA
ENST00000466620.5:n.2503_2504insAGA
ENST00000483362.1:n.1865_1866insAGA
ENST00000619289.4:c.*500_*501insAGA	ENSP00000484600.1:n.*500_*501insAGA
NM_001282447.1:c.*500_*501insAGA	NP_001269376.1:n.*500_*501insAGA
NM_025220.3:c.*500_*501insAGA	NP_079496.1:n.*500_*501insAGA
NM_153202.2:c.*500_*501insAGA	NP_694882.1:n.*500_*501insAGA
XM_005260843.1:c.*500_*501insAGA	XP_005260900.1:n.*500_*501insAGA
XM_006723639.1:c.*500_*501insAGA	XP_006723702.1:n.*500_*501insAGA
XM_006723640.1:c.*500_*501insAGA	XP_006723703.1:n.*500_*501insAGA
XM_011529366.1:c.*500_*501insAGA	XP_011527668.1:n.*500_*501insAGA
XM_011529367.1:c.*500_*501insAGA	XP_011527669.1:n.*500_*501insAGA
XM_011529368.1:c.*500_*501insAGA	XP_011527670.1:n.*500_*501insAGA
XM_011529373.1:c.*500_*501insAGA	XP_011527675.1:n.*500_*501insAGA
XR_937153.1:n.2963_2964insAGA
XR_937154.1:n.2963_2964insAGA
XR_937155.1:n.2884_2885insAGA
XR_937157.1:n.2886_2887insAGA
NM_001282447.2:c.*500_*501insAGA	NP_001269376.1:n.*500_*501insAGA
NM_025220.4:c.*500_*501insAGA	NP_079496.1:n.*500_*501insAGA
NM_153202.3:c.*500_*501insAGA	NP_694882.1:n.*500_*501insAGA
XM_011529373.2:c.*500_*501insAGA	XP_011527675.1:n.*500_*501insAGA
XR_001754405.1:n.3050_3051insAGA
XR_002958534.1:n.3159_3160insAGA
NM_001282447.3:c.*500_*501insAGA	NP_001269376.1:n.*500_*501insAGA
NM_025220.5:c.*500_*501insAGA MANE Select	NP_079496.1:n.*500_*501insAGA
NM_153202.4:c.*500_*501insAGA	NP_694882.1:n.*500_*501insAGA