Canonical Allele Identifier: CA408104762

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652110A>C (hg19) ; chr20:g.3671463A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671463A>C , CM000682.2:g.3671463A>C	GRCh38
NC_000020.10:g.3652110A>C , CM000682.1:g.3652110A>C	GRCh37
NC_000020.9:g.3600110A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.1939T>G MANE Select	ENSP00000348912.3:p.Phe647Val
ENST00000350009.6:c.1906-118T>G	ENSP00000322550.5:n.1906-118T>G
ENST00000356518.6:c.1939T>G	ENSP00000348912.2:p.Phe647Val
ENST00000379861.8:c.1939T>G	ENSP00000369190.4:p.Phe647Val
ENST00000466620.5:n.1545-118T>G
ENST00000617732.1:c.*632-6T>G	ENSP00000483343.1:n.*632-6T>G
ENST00000619289.4:c.1579T>G	ENSP00000484600.1:p.Phe527Val
NM_001282447.1:c.1939T>G	NP_001269376.1:p.Phe647Val
NM_025220.3:c.1939T>G	NP_079496.1:p.Phe647Val
NM_153202.2:c.1906-118T>G	NP_694882.1:n.1906-118T>G
XM_005260843.1:c.1978T>G	XP_005260900.1:p.Phe660Val
XM_006723639.1:c.1978T>G	XP_006723702.1:p.Phe660Val
XM_006723640.1:c.1969T>G	XP_006723703.1:p.Phe657Val
XM_011529366.1:c.1975T>G	XP_011527668.1:p.Phe659Val
XM_011529367.1:c.1936T>G	XP_011527669.1:p.Phe646Val
XM_011529368.1:c.1945-118T>G	XP_011527670.1:n.1945-118T>G
XM_011529369.1:c.*38T>G	XP_011527671.1:n.*38T>G
XM_011529370.1:c.*5-118T>G	XP_011527672.1:n.*5-118T>G
XM_011529373.1:c.976T>G	XP_011527675.1:p.Phe326Val
XR_937151.1:n.2082T>G
XR_937152.1:n.2082T>G
XR_937153.1:n.1963T>G
XR_937154.1:n.1963T>G
XR_937155.1:n.1884T>G
XR_937157.1:n.1886T>G
NM_001282447.2:c.1939T>G	NP_001269376.1:p.Phe647Val
NM_025220.4:c.1939T>G	NP_079496.1:p.Phe647Val
NM_153202.3:c.1906-118T>G	NP_694882.1:n.1906-118T>G
XM_011529373.2:c.976T>G	XP_011527675.1:p.Phe326Val
XR_001754405.1:n.2050T>G
XR_002958534.1:n.2159T>G
NM_001282447.3:c.1939T>G	NP_001269376.1:p.Phe647Val
NM_025220.5:c.1939T>G MANE Select	NP_079496.1:p.Phe647Val
NM_153202.4:c.1906-118T>G	NP_694882.1:n.1906-118T>G