Canonical Allele Identifier: CA2815082306

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668137_3668272del , CM000682.2:g.3668137_3668272del	GRCh38
NC_000020.10:g.3648784_3648919del , CM000682.1:g.3648784_3648919del	GRCh37
NC_000020.9:g.3596784_3596919del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.*701_*836del MANE Select	ENSP00000348912.3:n.*701_*836del
ENST00000350009.6:c.*701_*836del	ENSP00000322550.5:n.*701_*836del
ENST00000356518.6:c.*701_*836del	ENSP00000348912.2:n.*701_*836del
ENST00000379861.8:c.*701_*836del	ENSP00000369190.4:n.*701_*836del
ENST00000466620.5:n.2704_2839del
ENST00000483362.1:n.2066_2201del
ENST00000619289.4:c.*701_*836del	ENSP00000484600.1:n.*701_*836del
NM_001282447.1:c.*701_*836del	NP_001269376.1:n.*701_*836del
NM_025220.3:c.*701_*836del	NP_079496.1:n.*701_*836del
NM_153202.2:c.*701_*836del	NP_694882.1:n.*701_*836del
XM_005260843.1:c.*701_*836del	XP_005260900.1:n.*701_*836del
XM_006723639.1:c.*701_*836del	XP_006723702.1:n.*701_*836del
XM_006723640.1:c.*701_*836del	XP_006723703.1:n.*701_*836del
XM_011529366.1:c.*701_*836del	XP_011527668.1:n.*701_*836del
XM_011529367.1:c.*701_*836del	XP_011527669.1:n.*701_*836del
XM_011529368.1:c.*701_*836del	XP_011527670.1:n.*701_*836del
XM_011529373.1:c.*701_*836del	XP_011527675.1:n.*701_*836del
XR_937153.1:n.3164_3299del
XR_937154.1:n.3164_3299del
XR_937155.1:n.3085_3220del
XR_937157.1:n.3087_3222del
NM_001282447.2:c.*701_*836del	NP_001269376.1:n.*701_*836del
NM_025220.4:c.*701_*836del	NP_079496.1:n.*701_*836del
NM_153202.3:c.*701_*836del	NP_694882.1:n.*701_*836del
XM_011529373.2:c.*701_*836del	XP_011527675.1:n.*701_*836del
XR_001754405.1:n.3251_3386del
XR_002958534.1:n.3360_3495del
NM_001282447.3:c.*701_*836del	NP_001269376.1:n.*701_*836del
NM_025220.5:c.*701_*836del MANE Select	NP_079496.1:n.*701_*836del
NM_153202.4:c.*701_*836del	NP_694882.1:n.*701_*836del