Canonical Allele Identifier: CA744011018

Gene: ADAM33

Linked Data

• dbSNP Id: rs1244978180
• gnomAD v3: 20-3668324-T-TGAGG
• gnomAD v4: 20-3668324-T-TGAGG
• MyVariant Identifiers: chr20:g.3648971_3648972insGAGG (hg19) ; chr20:g.3668324_3668325insGAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668325_3668326insAGGG , CM000682.2:g.3668325_3668326insAGGG	GRCh38
NC_000020.10:g.3648972_3648973insAGGG , CM000682.1:g.3648972_3648973insAGGG	GRCh37
NC_000020.9:g.3596972_3596973insAGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.*638_*639insCCTC MANE Select	ENSP00000348912.3:n.*638_*639insCCTC
ENST00000350009.6:c.*638_*639insCCTC	ENSP00000322550.5:n.*638_*639insCCTC
ENST00000356518.6:c.*638_*639insCCTC	ENSP00000348912.2:n.*638_*639insCCTC
ENST00000379861.8:c.*638_*639insCCTC	ENSP00000369190.4:n.*638_*639insCCTC
ENST00000466620.5:n.2641_2642insCCTC
ENST00000483362.1:n.2003_2004insCCTC
ENST00000619289.4:c.*638_*639insCCTC	ENSP00000484600.1:n.*638_*639insCCTC
NM_001282447.1:c.*638_*639insCCTC	NP_001269376.1:n.*638_*639insCCTC
NM_025220.3:c.*638_*639insCCTC	NP_079496.1:n.*638_*639insCCTC
NM_153202.2:c.*638_*639insCCTC	NP_694882.1:n.*638_*639insCCTC
XM_005260843.1:c.*638_*639insCCTC	XP_005260900.1:n.*638_*639insCCTC
XM_006723639.1:c.*638_*639insCCTC	XP_006723702.1:n.*638_*639insCCTC
XM_006723640.1:c.*638_*639insCCTC	XP_006723703.1:n.*638_*639insCCTC
XM_011529366.1:c.*638_*639insCCTC	XP_011527668.1:n.*638_*639insCCTC
XM_011529367.1:c.*638_*639insCCTC	XP_011527669.1:n.*638_*639insCCTC
XM_011529368.1:c.*638_*639insCCTC	XP_011527670.1:n.*638_*639insCCTC
XM_011529373.1:c.*638_*639insCCTC	XP_011527675.1:n.*638_*639insCCTC
XR_937153.1:n.3101_3102insCCTC
XR_937154.1:n.3101_3102insCCTC
XR_937155.1:n.3022_3023insCCTC
XR_937157.1:n.3024_3025insCCTC
NM_001282447.2:c.*638_*639insCCTC	NP_001269376.1:n.*638_*639insCCTC
NM_025220.4:c.*638_*639insCCTC	NP_079496.1:n.*638_*639insCCTC
NM_153202.3:c.*638_*639insCCTC	NP_694882.1:n.*638_*639insCCTC
XM_011529373.2:c.*638_*639insCCTC	XP_011527675.1:n.*638_*639insCCTC
XR_001754405.1:n.3188_3189insCCTC
XR_002958534.1:n.3297_3298insCCTC
NM_001282447.3:c.*638_*639insCCTC	NP_001269376.1:n.*638_*639insCCTC
NM_025220.5:c.*638_*639insCCTC MANE Select	NP_079496.1:n.*638_*639insCCTC
NM_153202.4:c.*638_*639insCCTC	NP_694882.1:n.*638_*639insCCTC