Canonical Allele Identifier: CA2346677049

Gene: ADAM33

Linked Data

• dbSNP Id: rs2087328971

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668335_3668336insGGGAAGAG , CM000682.2:g.3668335_3668336insGGGAAGAG	GRCh38
NC_000020.10:g.3648982_3648983insGGGAAGAG , CM000682.1:g.3648982_3648983insGGGAAGAG	GRCh37
NC_000020.9:g.3596982_3596983insGGGAAGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.*628_*629insTCTTCCCC MANE Select	ENSP00000348912.3:n.*628_*629insTCTTCCCC
ENST00000350009.6:c.*628_*629insTCTTCCCC	ENSP00000322550.5:n.*628_*629insTCTTCCCC
ENST00000356518.6:c.*628_*629insTCTTCCCC	ENSP00000348912.2:n.*628_*629insTCTTCCCC
ENST00000379861.8:c.*628_*629insTCTTCCCC	ENSP00000369190.4:n.*628_*629insTCTTCCCC
ENST00000466620.5:n.2631_2632insTCTTCCCC
ENST00000483362.1:n.1993_1994insTCTTCCCC
ENST00000619289.4:c.*628_*629insTCTTCCCC	ENSP00000484600.1:n.*628_*629insTCTTCCCC
NM_001282447.1:c.*628_*629insTCTTCCCC	NP_001269376.1:n.*628_*629insTCTTCCCC
NM_025220.3:c.*628_*629insTCTTCCCC	NP_079496.1:n.*628_*629insTCTTCCCC
NM_153202.2:c.*628_*629insTCTTCCCC	NP_694882.1:n.*628_*629insTCTTCCCC
XM_005260843.1:c.*628_*629insTCTTCCCC	XP_005260900.1:n.*628_*629insTCTTCCCC
XM_006723639.1:c.*628_*629insTCTTCCCC	XP_006723702.1:n.*628_*629insTCTTCCCC
XM_006723640.1:c.*628_*629insTCTTCCCC	XP_006723703.1:n.*628_*629insTCTTCCCC
XM_011529366.1:c.*628_*629insTCTTCCCC	XP_011527668.1:n.*628_*629insTCTTCCCC
XM_011529367.1:c.*628_*629insTCTTCCCC	XP_011527669.1:n.*628_*629insTCTTCCCC
XM_011529368.1:c.*628_*629insTCTTCCCC	XP_011527670.1:n.*628_*629insTCTTCCCC
XM_011529373.1:c.*628_*629insTCTTCCCC	XP_011527675.1:n.*628_*629insTCTTCCCC
XR_937153.1:n.3091_3092insTCTTCCCC
XR_937154.1:n.3091_3092insTCTTCCCC
XR_937155.1:n.3012_3013insTCTTCCCC
XR_937157.1:n.3014_3015insTCTTCCCC
NM_001282447.2:c.*628_*629insTCTTCCCC	NP_001269376.1:n.*628_*629insTCTTCCCC
NM_025220.4:c.*628_*629insTCTTCCCC	NP_079496.1:n.*628_*629insTCTTCCCC
NM_153202.3:c.*628_*629insTCTTCCCC	NP_694882.1:n.*628_*629insTCTTCCCC
XM_011529373.2:c.*628_*629insTCTTCCCC	XP_011527675.1:n.*628_*629insTCTTCCCC
XR_001754405.1:n.3178_3179insTCTTCCCC
XR_002958534.1:n.3287_3288insTCTTCCCC
NM_001282447.3:c.*628_*629insTCTTCCCC	NP_001269376.1:n.*628_*629insTCTTCCCC
NM_025220.5:c.*628_*629insTCTTCCCC MANE Select	NP_079496.1:n.*628_*629insTCTTCCCC
NM_153202.4:c.*628_*629insTCTTCCCC	NP_694882.1:n.*628_*629insTCTTCCCC