Canonical Allele Identifier: CA1014874050

Gene: ADAM33

Linked Data

• dbSNP Id: rs2087329506
• gnomAD v3: 20-3668342-C-CGGGAAGAG
• gnomAD v4: 20-3668342-C-CGGGAAGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668343_3668344insGGAAGAGG , CM000682.2:g.3668343_3668344insGGAAGAGG	GRCh38
NC_000020.10:g.3648990_3648991insGGAAGAGG , CM000682.1:g.3648990_3648991insGGAAGAGG	GRCh37
NC_000020.9:g.3596990_3596991insGGAAGAGG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.*620_*621insCTCTTCCC MANE Select	ENSP00000348912.3:n.*620_*621insCTCTTCCC
ENST00000350009.6:c.*620_*621insCTCTTCCC	ENSP00000322550.5:n.*620_*621insCTCTTCCC
ENST00000356518.6:c.*620_*621insCTCTTCCC	ENSP00000348912.2:n.*620_*621insCTCTTCCC
ENST00000379861.8:c.*620_*621insCTCTTCCC	ENSP00000369190.4:n.*620_*621insCTCTTCCC
ENST00000466620.5:n.2623_2624insCTCTTCCC
ENST00000483362.1:n.1985_1986insCTCTTCCC
ENST00000619289.4:c.*620_*621insCTCTTCCC	ENSP00000484600.1:n.*620_*621insCTCTTCCC
NM_001282447.1:c.*620_*621insCTCTTCCC	NP_001269376.1:n.*620_*621insCTCTTCCC
NM_025220.3:c.*620_*621insCTCTTCCC	NP_079496.1:n.*620_*621insCTCTTCCC
NM_153202.2:c.*620_*621insCTCTTCCC	NP_694882.1:n.*620_*621insCTCTTCCC
XM_005260843.1:c.*620_*621insCTCTTCCC	XP_005260900.1:n.*620_*621insCTCTTCCC
XM_006723639.1:c.*620_*621insCTCTTCCC	XP_006723702.1:n.*620_*621insCTCTTCCC
XM_006723640.1:c.*620_*621insCTCTTCCC	XP_006723703.1:n.*620_*621insCTCTTCCC
XM_011529366.1:c.*620_*621insCTCTTCCC	XP_011527668.1:n.*620_*621insCTCTTCCC
XM_011529367.1:c.*620_*621insCTCTTCCC	XP_011527669.1:n.*620_*621insCTCTTCCC
XM_011529368.1:c.*620_*621insCTCTTCCC	XP_011527670.1:n.*620_*621insCTCTTCCC
XM_011529373.1:c.*620_*621insCTCTTCCC	XP_011527675.1:n.*620_*621insCTCTTCCC
XR_937153.1:n.3083_3084insCTCTTCCC
XR_937154.1:n.3083_3084insCTCTTCCC
XR_937155.1:n.3004_3005insCTCTTCCC
XR_937157.1:n.3006_3007insCTCTTCCC
NM_001282447.2:c.*620_*621insCTCTTCCC	NP_001269376.1:n.*620_*621insCTCTTCCC
NM_025220.4:c.*620_*621insCTCTTCCC	NP_079496.1:n.*620_*621insCTCTTCCC
NM_153202.3:c.*620_*621insCTCTTCCC	NP_694882.1:n.*620_*621insCTCTTCCC
XM_011529373.2:c.*620_*621insCTCTTCCC	XP_011527675.1:n.*620_*621insCTCTTCCC
XR_001754405.1:n.3170_3171insCTCTTCCC
XR_002958534.1:n.3279_3280insCTCTTCCC
NM_001282447.3:c.*620_*621insCTCTTCCC	NP_001269376.1:n.*620_*621insCTCTTCCC
NM_025220.5:c.*620_*621insCTCTTCCC MANE Select	NP_079496.1:n.*620_*621insCTCTTCCC
NM_153202.4:c.*620_*621insCTCTTCCC	NP_694882.1:n.*620_*621insCTCTTCCC