Canonical Allele Identifier: CA2346677488

Gene: ADAM33

Linked Data

• dbSNP Id: rs2087363282

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669159_3669160insC , CM000682.2:g.3669159_3669160insC	GRCh38
NC_000020.10:g.3649806_3649807insC , CM000682.1:g.3649806_3649807insC	GRCh37
NC_000020.9:g.3597806_3597807insC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2404+139_2404+140insG MANE Select	ENSP00000348912.3:n.2404+139_2404+140insG...
ENST00000350009.6:c.2326+139_2326+140insG	ENSP00000322550.5:n.2326+139_2326+140insG...
ENST00000356518.6:c.2404+139_2404+140insG	ENSP00000348912.2:n.2404+139_2404+140insG...
ENST00000379861.8:c.2404+139_2404+140insG	ENSP00000369190.4:n.2404+139_2404+140insG...
ENST00000466620.5:n.1965+139_1965+140insG
ENST00000483362.1:n.1327+139_1327+140insG
ENST00000617732.1:c.*1091+139_*1091+140insG	ENSP00000483343.1:n.*1091+139_*1091+140in...
ENST00000619289.4:c.2044+139_2044+140insG	ENSP00000484600.1:n.2044+139_2044+140insG...
NM_001282447.1:c.2404+139_2404+140insG	NP_001269376.1:n.2404+139_2404+140insG
NM_025220.3:c.2404+139_2404+140insG	NP_079496.1:n.2404+139_2404+140insG
NM_153202.2:c.2326+139_2326+140insG	NP_694882.1:n.2326+139_2326+140insG
XM_005260843.1:c.2443+139_2443+140insG	XP_005260900.1:n.2443+139_2443+140insG
XM_006723639.1:c.2443+139_2443+140insG	XP_006723702.1:n.2443+139_2443+140insG
XM_006723640.1:c.2434+139_2434+140insG	XP_006723703.1:n.2434+139_2434+140insG
XM_011529366.1:c.2440+139_2440+140insG	XP_011527668.1:n.2440+139_2440+140insG
XM_011529367.1:c.2401+139_2401+140insG	XP_011527669.1:n.2401+139_2401+140insG
XM_011529368.1:c.2365+139_2365+140insG	XP_011527670.1:n.2365+139_2365+140insG
XM_011529373.1:c.1441+139_1441+140insG	XP_011527675.1:n.1441+139_1441+140insG
XR_937151.1:n.2455+139_2455+140insG
XR_937152.1:n.2455+139_2455+140insG
XR_937153.1:n.2428+139_2428+140insG
XR_937154.1:n.2428+139_2428+140insG
XR_937155.1:n.2349+139_2349+140insG
XR_937157.1:n.2351+139_2351+140insG
NM_001282447.2:c.2404+139_2404+140insG	NP_001269376.1:n.2404+139_2404+140insG
NM_025220.4:c.2404+139_2404+140insG	NP_079496.1:n.2404+139_2404+140insG
NM_153202.3:c.2326+139_2326+140insG	NP_694882.1:n.2326+139_2326+140insG
XM_011529373.2:c.1441+139_1441+140insG	XP_011527675.1:n.1441+139_1441+140insG
XR_001754405.1:n.2515+139_2515+140insG
XR_002958534.1:n.2624+139_2624+140insG
NM_001282447.3:c.2404+139_2404+140insG	NP_001269376.1:n.2404+139_2404+140insG
NM_025220.5:c.2404+139_2404+140insG MANE Select	NP_079496.1:n.2404+139_2404+140insG
NM_153202.4:c.2326+139_2326+140insG	NP_694882.1:n.2326+139_2326+140insG