Canonical Allele Identifier: CA645608882

Gene: ADAM33

Linked Data

• COSMIC: COSM4565590

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669607_3669608delinsAA , CM000682.2:g.3669607_3669608delinsAA	GRCh38
NC_000020.10:g.3650254_3650255delinsAA , CM000682.1:g.3650254_3650255delinsAA	GRCh37
NC_000020.9:g.3598254_3598255delinsAA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2270_2271delinsTT MANE Select	ENSP00000348912.3:p.Pro757Leu
ENST00000350009.6:c.2192_2193delinsTT	ENSP00000322550.5:p.Pro731Leu
ENST00000356518.6:c.2270_2271delinsTT	ENSP00000348912.2:p.Pro757Leu
ENST00000379861.8:c.2270_2271delinsTT	ENSP00000369190.4:p.Pro757Leu
ENST00000466620.5:n.1831_1832delinsTT
ENST00000483362.1:n.1018_1019delinsTT
ENST00000617732.1:c.*957_*958delinsTT	ENSP00000483343.1:n.*957_*958delinsTT
ENST00000619289.4:c.1910_1911delinsTT	ENSP00000484600.1:p.Pro637Leu
NM_001282447.1:c.2270_2271delinsTT	NP_001269376.1:p.Pro757Leu
NM_025220.3:c.2270_2271delinsTT	NP_079496.1:p.Pro757Leu
NM_153202.2:c.2192_2193delinsTT	NP_694882.1:p.Pro731Leu
XM_005260843.1:c.2309_2310delinsTT	XP_005260900.1:p.Pro770Leu
XM_006723639.1:c.2309_2310delinsTT	XP_006723702.1:p.Pro770Leu
XM_006723640.1:c.2300_2301delinsTT	XP_006723703.1:p.Pro767Leu
XM_011529366.1:c.2306_2307delinsTT	XP_011527668.1:p.Pro769Leu
XM_011529367.1:c.2267_2268delinsTT	XP_011527669.1:p.Pro756Leu
XM_011529368.1:c.2231_2232delinsTT	XP_011527670.1:p.Pro744Leu
XM_011529373.1:c.1307_1308delinsTT	XP_011527675.1:p.Pro436Leu
XR_937151.1:n.2384-238_2384-237delinsTT
XR_937152.1:n.2384-238_2384-237delinsTT
XR_937153.1:n.2294_2295delinsTT
XR_937154.1:n.2294_2295delinsTT
XR_937155.1:n.2215_2216delinsTT
XR_937157.1:n.2217_2218delinsTT
NM_001282447.2:c.2270_2271delinsTT	NP_001269376.1:p.Pro757Leu
NM_025220.4:c.2270_2271delinsTT	NP_079496.1:p.Pro757Leu
NM_153202.3:c.2192_2193delinsTT	NP_694882.1:p.Pro731Leu
XM_011529373.2:c.1307_1308delinsTT	XP_011527675.1:p.Pro436Leu
XR_001754405.1:n.2381_2382delinsTT
XR_002958534.1:n.2490_2491delinsTT
NM_001282447.3:c.2270_2271delinsTT	NP_001269376.1:p.Pro757Leu
NM_025220.5:c.2270_2271delinsTT MANE Select	NP_079496.1:p.Pro757Leu
NM_153202.4:c.2192_2193delinsTT	NP_694882.1:p.Pro731Leu