Canonical Allele Identifier: CA509419243

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650221G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669574G>C , CM000682.2:g.3669574G>C	GRCh38
NC_000020.10:g.3650221G>C , CM000682.1:g.3650221G>C	GRCh37
NC_000020.9:g.3598221G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2304C>G MANE Select	ENSP00000348912.3:p.Pro768=
ENST00000350009.6:c.2226C>G	ENSP00000322550.5:p.Pro742=
ENST00000356518.6:c.2304C>G	ENSP00000348912.2:p.Pro768=
ENST00000379861.8:c.2304C>G	ENSP00000369190.4:p.Pro768=
ENST00000466620.5:n.1865C>G
ENST00000483362.1:n.1052C>G
ENST00000617732.1:c.*991C>G	ENSP00000483343.1:n.*991C>G
ENST00000619289.4:c.1944C>G	ENSP00000484600.1:p.Pro648=
NM_001282447.1:c.2304C>G	NP_001269376.1:p.Pro768=
NM_025220.3:c.2304C>G	NP_079496.1:p.Pro768=
NM_153202.2:c.2226C>G	NP_694882.1:p.Pro742=
XM_005260843.1:c.2343C>G	XP_005260900.1:p.Pro781=
XM_006723639.1:c.2343C>G	XP_006723702.1:p.Pro781=
XM_006723640.1:c.2334C>G	XP_006723703.1:p.Pro778=
XM_011529366.1:c.2340C>G	XP_011527668.1:p.Pro780=
XM_011529367.1:c.2301C>G	XP_011527669.1:p.Pro767=
XM_011529368.1:c.2265C>G	XP_011527670.1:p.Pro755=
XM_011529373.1:c.1341C>G	XP_011527675.1:p.Pro447=
XR_937151.1:n.2384-204C>G
XR_937152.1:n.2384-204C>G
XR_937153.1:n.2328C>G
XR_937154.1:n.2328C>G
XR_937155.1:n.2249C>G
XR_937157.1:n.2251C>G
NM_001282447.2:c.2304C>G	NP_001269376.1:p.Pro768=
NM_025220.4:c.2304C>G	NP_079496.1:p.Pro768=
NM_153202.3:c.2226C>G	NP_694882.1:p.Pro742=
XM_011529373.2:c.1341C>G	XP_011527675.1:p.Pro447=
XR_001754405.1:n.2415C>G
XR_002958534.1:n.2524C>G
NM_001282447.3:c.2304C>G	NP_001269376.1:p.Pro768=
NM_025220.5:c.2304C>G MANE Select	NP_079496.1:p.Pro768=
NM_153202.4:c.2226C>G	NP_694882.1:p.Pro742=