Canonical Allele Identifier: CA744010795

Gene: ADAM33

Linked Data

• dbSNP Id: rs1254383893
• MyVariant Identifiers: chr20:g.3648619_3648620del (hg19) ; chr20:g.3667972_3667973del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3667974_3667975del , CM000682.2:g.3667974_3667975del	GRCh38
NC_000020.10:g.3648621_3648622del , CM000682.1:g.3648621_3648622del	GRCh37
NC_000020.9:g.3596621_3596622del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.6:c.*990_*991del	ENSP00000348912.2:n.*990_*991del
ENST00000379861.8:c.*990_*991del	ENSP00000369190.4:n.*990_*991del
ENST00000466620.5:n.2993_2994del
ENST00000483362.1:n.2355_2356del
NM_001282447.2:c.*990_*991del	NP_001269376.1:n.*990_*991del
NM_025220.4:c.*990_*991del	NP_079496.1:n.*990_*991del
NM_153202.3:c.*990_*991del	NP_694882.1:n.*990_*991del