Canonical Allele Identifier: CA2346677486

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669157_3669158delinsCA , CM000682.2:g.3669157_3669158delinsCA	GRCh38
NC_000020.10:g.3649804_3649805delinsCA , CM000682.1:g.3649804_3649805delinsCA	GRCh37
NC_000020.9:g.3597804_3597805delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2404+141_2404+142delinsTG MANE Select	ENSP00000348912.3:n.2404+141_2404+142deli...
ENST00000350009.6:c.2326+141_2326+142delinsTG	ENSP00000322550.5:n.2326+141_2326+142deli...
ENST00000356518.6:c.2404+141_2404+142delinsTG	ENSP00000348912.2:n.2404+141_2404+142deli...
ENST00000379861.8:c.2404+141_2404+142delinsTG	ENSP00000369190.4:n.2404+141_2404+142deli...
ENST00000466620.5:n.1965+141_1965+142delinsTG
ENST00000483362.1:n.1327+141_1327+142delinsTG
ENST00000617732.1:c.*1091+141_*1091+142delinsTG	ENSP00000483343.1:n.*1091+141_*1091+142de...
ENST00000619289.4:c.2044+141_2044+142delinsTG	ENSP00000484600.1:n.2044+141_2044+142deli...
NM_001282447.1:c.2404+141_2404+142delinsTG	NP_001269376.1:n.2404+141_2404+142delinsT...
NM_025220.3:c.2404+141_2404+142delinsTG	NP_079496.1:n.2404+141_2404+142delinsTG
NM_153202.2:c.2326+141_2326+142delinsTG	NP_694882.1:n.2326+141_2326+142delinsTG
XM_005260843.1:c.2443+141_2443+142delinsTG	XP_005260900.1:n.2443+141_2443+142delinsT...
XM_006723639.1:c.2443+141_2443+142delinsTG	XP_006723702.1:n.2443+141_2443+142delinsT...
XM_006723640.1:c.2434+141_2434+142delinsTG	XP_006723703.1:n.2434+141_2434+142delinsT...
XM_011529366.1:c.2440+141_2440+142delinsTG	XP_011527668.1:n.2440+141_2440+142delinsT...
XM_011529367.1:c.2401+141_2401+142delinsTG	XP_011527669.1:n.2401+141_2401+142delinsT...
XM_011529368.1:c.2365+141_2365+142delinsTG	XP_011527670.1:n.2365+141_2365+142delinsT...
XM_011529373.1:c.1441+141_1441+142delinsTG	XP_011527675.1:n.1441+141_1441+142delinsT...
XR_937151.1:n.2455+141_2455+142delinsTG
XR_937152.1:n.2455+141_2455+142delinsTG
XR_937153.1:n.2428+141_2428+142delinsTG
XR_937154.1:n.2428+141_2428+142delinsTG
XR_937155.1:n.2349+141_2349+142delinsTG
XR_937157.1:n.2351+141_2351+142delinsTG
NM_001282447.2:c.2404+141_2404+142delinsTG	NP_001269376.1:n.2404+141_2404+142delinsT...
NM_025220.4:c.2404+141_2404+142delinsTG	NP_079496.1:n.2404+141_2404+142delinsTG
NM_153202.3:c.2326+141_2326+142delinsTG	NP_694882.1:n.2326+141_2326+142delinsTG
XM_011529373.2:c.1441+141_1441+142delinsTG	XP_011527675.1:n.1441+141_1441+142delinsT...
XR_001754405.1:n.2515+141_2515+142delinsTG
XR_002958534.1:n.2624+141_2624+142delinsTG
NM_001282447.3:c.2404+141_2404+142delinsTG	NP_001269376.1:n.2404+141_2404+142delinsT...
NM_025220.5:c.2404+141_2404+142delinsTG MANE Select	NP_079496.1:n.2404+141_2404+142delinsTG
NM_153202.4:c.2326+141_2326+142delinsTG	NP_694882.1:n.2326+141_2326+142delinsTG