Canonical Allele Identifier: CA2346677211

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668626_3668639delinsCCAGACTCCCAGGA , CM000682.2:g.3668626_3668639delinsCCAGACTCCCAGGA	GRCh38
NC_000020.10:g.3649273_3649286delinsCCAGACTCCCAGGA , CM000682.1:g.3649273_3649286delinsCCAGACTCCCAGGA	GRCh37
NC_000020.9:g.3597273_3597286delinsCCAGACTCCCAGGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.*324_*337delinsTCCTGGGAGTCTGG MANE Select	ENSP00000348912.3:n.*324_*337delinsTCCTGGGAGTCTGG
ENST00000350009.6:c.*324_*337delinsTCCTGGGAGTCTGG	ENSP00000322550.5:n.*324_*337delinsTCCTGGGAGTCTGG
ENST00000356518.6:c.*324_*337delinsTCCTGGGAGTCTGG	ENSP00000348912.2:n.*324_*337delinsTCCTGGGAGTCTGG
ENST00000379861.8:c.*324_*337delinsTCCTGGGAGTCTGG	ENSP00000369190.4:n.*324_*337delinsTCCTGGGAGTCTGG
ENST00000466620.5:n.2327_2340delinsTCCTGGGAGTCTGG
ENST00000483362.1:n.1689_1702delinsTCCTGGGAGTCTGG
ENST00000617732.1:c.*1450_*1463delinsTCCTGGGAGTCTGG	ENSP00000483343.1:n.*1450_*1463delinsTCCTGGGAGTCTGG
ENST00000619289.4:c.*324_*337delinsTCCTGGGAGTCTGG	ENSP00000484600.1:n.*324_*337delinsTCCTGGGAGTCTGG
NM_001282447.1:c.*324_*337delinsTCCTGGGAGTCTGG	NP_001269376.1:n.*324_*337delinsTCCTGGGAGTCTGG
NM_025220.3:c.*324_*337delinsTCCTGGGAGTCTGG	NP_079496.1:n.*324_*337delinsTCCTGGGAGTCTGG
NM_153202.2:c.*324_*337delinsTCCTGGGAGTCTGG	NP_694882.1:n.*324_*337delinsTCCTGGGAGTCTGG
XM_005260843.1:c.*324_*337delinsTCCTGGGAGTCTGG	XP_005260900.1:n.*324_*337delinsTCCTGGGAGTCTGG
XM_006723639.1:c.*324_*337delinsTCCTGGGAGTCTGG	XP_006723702.1:n.*324_*337delinsTCCTGGGAGTCTGG
XM_006723640.1:c.*324_*337delinsTCCTGGGAGTCTGG	XP_006723703.1:n.*324_*337delinsTCCTGGGAGTCTGG
XM_011529366.1:c.*324_*337delinsTCCTGGGAGTCTGG	XP_011527668.1:n.*324_*337delinsTCCTGGGAGTCTGG
XM_011529367.1:c.*324_*337delinsTCCTGGGAGTCTGG	XP_011527669.1:n.*324_*337delinsTCCTGGGAGTCTGG
XM_011529368.1:c.*324_*337delinsTCCTGGGAGTCTGG	XP_011527670.1:n.*324_*337delinsTCCTGGGAGTCTGG
XM_011529373.1:c.*324_*337delinsTCCTGGGAGTCTGG	XP_011527675.1:n.*324_*337delinsTCCTGGGAGTCTGG
XR_937153.1:n.2787_2800delinsTCCTGGGAGTCTGG
XR_937154.1:n.2787_2800delinsTCCTGGGAGTCTGG
XR_937155.1:n.2708_2721delinsTCCTGGGAGTCTGG
XR_937157.1:n.2710_2723delinsTCCTGGGAGTCTGG
NM_001282447.2:c.*324_*337delinsTCCTGGGAGTCTGG	NP_001269376.1:n.*324_*337delinsTCCTGGGAGTCTGG
NM_025220.4:c.*324_*337delinsTCCTGGGAGTCTGG	NP_079496.1:n.*324_*337delinsTCCTGGGAGTCTGG
NM_153202.3:c.*324_*337delinsTCCTGGGAGTCTGG	NP_694882.1:n.*324_*337delinsTCCTGGGAGTCTGG
XM_011529373.2:c.*324_*337delinsTCCTGGGAGTCTGG	XP_011527675.1:n.*324_*337delinsTCCTGGGAGTCTGG
XR_001754405.1:n.2874_2887delinsTCCTGGGAGTCTGG
XR_002958534.1:n.2983_2996delinsTCCTGGGAGTCTGG
NM_001282447.3:c.*324_*337delinsTCCTGGGAGTCTGG	NP_001269376.1:n.*324_*337delinsTCCTGGGAGTCTGG
NM_025220.5:c.*324_*337delinsTCCTGGGAGTCTGG MANE Select	NP_079496.1:n.*324_*337delinsTCCTGGGAGTCTGG
NM_153202.4:c.*324_*337delinsTCCTGGGAGTCTGG	NP_694882.1:n.*324_*337delinsTCCTGGGAGTCTGG