Canonical Allele Identifier: CA408104733

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652098G>T (hg19) ; chr20:g.3671451G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671451G>T , CM000682.2:g.3671451G>T	GRCh38
NC_000020.10:g.3652098G>T , CM000682.1:g.3652098G>T	GRCh37
NC_000020.9:g.3600098G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1951C>A MANE Select	ENSP00000348912.3:p.Gln651Lys
ENST00000350009.6:c.1906-106C>A	ENSP00000322550.5:n.1906-106C>A
ENST00000356518.6:c.1951C>A	ENSP00000348912.2:p.Gln651Lys
ENST00000379861.8:c.1951C>A	ENSP00000369190.4:p.Gln651Lys
ENST00000466620.5:n.1545-106C>A
ENST00000617732.1:c.*638C>A	ENSP00000483343.1:n.*638C>A
ENST00000619289.4:c.1591C>A	ENSP00000484600.1:p.Gln531Lys
NM_001282447.1:c.1951C>A	NP_001269376.1:p.Gln651Lys
NM_025220.3:c.1951C>A	NP_079496.1:p.Gln651Lys
NM_153202.2:c.1906-106C>A	NP_694882.1:n.1906-106C>A
XM_005260843.1:c.1990C>A	XP_005260900.1:p.Gln664Lys
XM_006723639.1:c.1990C>A	XP_006723702.1:p.Gln664Lys
XM_006723640.1:c.1981C>A	XP_006723703.1:p.Gln661Lys
XM_011529366.1:c.1987C>A	XP_011527668.1:p.Gln663Lys
XM_011529367.1:c.1948C>A	XP_011527669.1:p.Gln650Lys
XM_011529368.1:c.1945-106C>A	XP_011527670.1:n.1945-106C>A
XM_011529369.1:c.*50C>A	XP_011527671.1:n.*50C>A
XM_011529370.1:c.*5-106C>A	XP_011527672.1:n.*5-106C>A
XM_011529373.1:c.988C>A	XP_011527675.1:p.Gln330Lys
XR_937151.1:n.2094C>A
XR_937152.1:n.2094C>A
XR_937153.1:n.1975C>A
XR_937154.1:n.1975C>A
XR_937155.1:n.1896C>A
XR_937157.1:n.1898C>A
NM_001282447.2:c.1951C>A	NP_001269376.1:p.Gln651Lys
NM_025220.4:c.1951C>A	NP_079496.1:p.Gln651Lys
NM_153202.3:c.1906-106C>A	NP_694882.1:n.1906-106C>A
XM_011529373.2:c.988C>A	XP_011527675.1:p.Gln330Lys
XR_001754405.1:n.2062C>A
XR_002958534.1:n.2171C>A
NM_001282447.3:c.1951C>A	NP_001269376.1:p.Gln651Lys
NM_025220.5:c.1951C>A MANE Select	NP_079496.1:p.Gln651Lys
NM_153202.4:c.1906-106C>A	NP_694882.1:n.1906-106C>A