Canonical Allele Identifier: CA744011141

Gene: ADAM33

Linked Data

• dbSNP Id: rs1446130391
• MyVariant Identifiers: chr20:g.3649111_3649114del (hg19) ; chr20:g.3668464_3668467del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668471_3668474del , CM000682.2:g.3668471_3668474del	GRCh38
NC_000020.10:g.3649118_3649121del , CM000682.1:g.3649118_3649121del	GRCh37
NC_000020.9:g.3597118_3597121del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.*496_*499del MANE Select	ENSP00000348912.3:n.*496_*499del
ENST00000350009.6:c.*496_*499del	ENSP00000322550.5:n.*496_*499del
ENST00000356518.6:c.*496_*499del	ENSP00000348912.2:n.*496_*499del
ENST00000379861.8:c.*496_*499del	ENSP00000369190.4:n.*496_*499del
ENST00000466620.5:n.2499_2502del
ENST00000483362.1:n.1861_1864del
ENST00000619289.4:c.*496_*499del	ENSP00000484600.1:n.*496_*499del
NM_001282447.1:c.*496_*499del	NP_001269376.1:n.*496_*499del
NM_025220.3:c.*496_*499del	NP_079496.1:n.*496_*499del
NM_153202.2:c.*496_*499del	NP_694882.1:n.*496_*499del
XM_005260843.1:c.*496_*499del	XP_005260900.1:n.*496_*499del
XM_006723639.1:c.*496_*499del	XP_006723702.1:n.*496_*499del
XM_006723640.1:c.*496_*499del	XP_006723703.1:n.*496_*499del
XM_011529366.1:c.*496_*499del	XP_011527668.1:n.*496_*499del
XM_011529367.1:c.*496_*499del	XP_011527669.1:n.*496_*499del
XM_011529368.1:c.*496_*499del	XP_011527670.1:n.*496_*499del
XM_011529373.1:c.*496_*499del	XP_011527675.1:n.*496_*499del
XR_937153.1:n.2959_2962del
XR_937154.1:n.2959_2962del
XR_937155.1:n.2880_2883del
XR_937157.1:n.2882_2885del
NM_001282447.2:c.*496_*499del	NP_001269376.1:n.*496_*499del
NM_025220.4:c.*496_*499del	NP_079496.1:n.*496_*499del
NM_153202.3:c.*496_*499del	NP_694882.1:n.*496_*499del
XM_011529373.2:c.*496_*499del	XP_011527675.1:n.*496_*499del
XR_001754405.1:n.3046_3049del
XR_002958534.1:n.3155_3158del
NM_001282447.3:c.*496_*499del	NP_001269376.1:n.*496_*499del
NM_025220.5:c.*496_*499del MANE Select	NP_079496.1:n.*496_*499del
NM_153202.4:c.*496_*499del	NP_694882.1:n.*496_*499del