Canonical Allele Identifier: CA2346676891

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3667971_3667973delinsAAT , CM000682.2:g.3667971_3667973delinsAAT	GRCh38
NC_000020.10:g.3648618_3648620delinsAAT , CM000682.1:g.3648618_3648620delinsAAT	GRCh37
NC_000020.9:g.3596618_3596620delinsAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.6:c.*990_*992delinsATT	ENSP00000348912.2:n.*990_*992delinsATT
ENST00000379861.8:c.*990_*992delinsATT	ENSP00000369190.4:n.*990_*992delinsATT
ENST00000466620.5:n.2993_2995delinsATT
ENST00000483362.1:n.2355_2357delinsATT
NM_001282447.2:c.*990_*992delinsATT	NP_001269376.1:n.*990_*992delinsATT
NM_025220.4:c.*990_*992delinsATT	NP_079496.1:n.*990_*992delinsATT
NM_153202.3:c.*990_*992delinsATT	NP_694882.1:n.*990_*992delinsATT