Canonical Allele Identifier: CA310997332

Gene: ADAM33

Linked Data

• dbSNP Id: rs934896255
• gnomAD v3: 20-3668486-ATGTT-A
• gnomAD v4: 20-3668486-ATGTT-A
• MyVariant Identifiers: chr20:g.3649134_3649137del (hg19) ; chr20:g.3668487_3668490del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668493_3668496del , CM000682.2:g.3668493_3668496del	GRCh38
NC_000020.10:g.3649140_3649143del , CM000682.1:g.3649140_3649143del	GRCh37
NC_000020.9:g.3597140_3597143del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.*473_*476del MANE Select	ENSP00000348912.3:n.*473_*476del
ENST00000350009.6:c.*473_*476del	ENSP00000322550.5:n.*473_*476del
ENST00000356518.6:c.*473_*476del	ENSP00000348912.2:n.*473_*476del
ENST00000379861.8:c.*473_*476del	ENSP00000369190.4:n.*473_*476del
ENST00000466620.5:n.2476_2479del
ENST00000483362.1:n.1838_1841del
ENST00000619289.4:c.*473_*476del	ENSP00000484600.1:n.*473_*476del
NM_001282447.1:c.*473_*476del	NP_001269376.1:n.*473_*476del
NM_025220.3:c.*473_*476del	NP_079496.1:n.*473_*476del
NM_153202.2:c.*473_*476del	NP_694882.1:n.*473_*476del
XM_005260843.1:c.*473_*476del	XP_005260900.1:n.*473_*476del
XM_006723639.1:c.*473_*476del	XP_006723702.1:n.*473_*476del
XM_006723640.1:c.*473_*476del	XP_006723703.1:n.*473_*476del
XM_011529366.1:c.*473_*476del	XP_011527668.1:n.*473_*476del
XM_011529367.1:c.*473_*476del	XP_011527669.1:n.*473_*476del
XM_011529368.1:c.*473_*476del	XP_011527670.1:n.*473_*476del
XM_011529373.1:c.*473_*476del	XP_011527675.1:n.*473_*476del
XR_937153.1:n.2936_2939del
XR_937154.1:n.2936_2939del
XR_937155.1:n.2857_2860del
XR_937157.1:n.2859_2862del
NM_001282447.2:c.*473_*476del	NP_001269376.1:n.*473_*476del
NM_025220.4:c.*473_*476del	NP_079496.1:n.*473_*476del
NM_153202.3:c.*473_*476del	NP_694882.1:n.*473_*476del
XM_011529373.2:c.*473_*476del	XP_011527675.1:n.*473_*476del
XR_001754405.1:n.3023_3026del
XR_002958534.1:n.3132_3135del
NM_001282447.3:c.*473_*476del	NP_001269376.1:n.*473_*476del
NM_025220.5:c.*473_*476del MANE Select	NP_079496.1:n.*473_*476del
NM_153202.4:c.*473_*476del	NP_694882.1:n.*473_*476del