Canonical Allele Identifier: CA509559888

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652294G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671647G>C , CM000682.2:g.3671647G>C	GRCh38
NC_000020.10:g.3652294G>C , CM000682.1:g.3652294G>C	GRCh37
NC_000020.9:g.3600294G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1839C>G MANE Select	ENSP00000348912.3:p.Pro613=
ENST00000350009.6:c.1839C>G	ENSP00000322550.5:p.Pro613=
ENST00000356518.6:c.1839C>G	ENSP00000348912.2:p.Pro613=
ENST00000379861.8:c.1839C>G	ENSP00000369190.4:p.Pro613=
ENST00000466620.5:n.1478C>G
ENST00000617732.1:c.*632-190C>G	ENSP00000483343.1:n.*632-190C>G
ENST00000619289.4:c.1479C>G	ENSP00000484600.1:p.Pro493=
NM_001282447.1:c.1839C>G	NP_001269376.1:p.Pro613=
NM_025220.3:c.1839C>G	NP_079496.1:p.Pro613=
NM_153202.2:c.1839C>G	NP_694882.1:p.Pro613=
XM_005260843.1:c.1878C>G	XP_005260900.1:p.Pro626=
XM_006723639.1:c.1878C>G	XP_006723702.1:p.Pro626=
XM_006723640.1:c.1869C>G	XP_006723703.1:p.Pro623=
XM_011529366.1:c.1875C>G	XP_011527668.1:p.Pro625=
XM_011529367.1:c.1836C>G	XP_011527669.1:p.Pro612=
XM_011529368.1:c.1878C>G	XP_011527670.1:p.Pro626=
XM_011529369.1:c.1846C>G	XP_011527671.1:p.Gln616Glu
XM_011529370.1:c.1846C>G	XP_011527672.1:p.Gln616Glu
XM_011529373.1:c.876C>G	XP_011527675.1:p.Pro292=
XR_937151.1:n.1982C>G
XR_937152.1:n.1982C>G
XR_937153.1:n.1863C>G
XR_937154.1:n.1863C>G
XR_937155.1:n.1784C>G
XR_937157.1:n.1786C>G
NM_001282447.2:c.1839C>G	NP_001269376.1:p.Pro613=
NM_025220.4:c.1839C>G	NP_079496.1:p.Pro613=
NM_153202.3:c.1839C>G	NP_694882.1:p.Pro613=
XM_011529373.2:c.876C>G	XP_011527675.1:p.Pro292=
XR_001754405.1:n.1950C>G
XR_002958534.1:n.2059C>G
NM_001282447.3:c.1839C>G	NP_001269376.1:p.Pro613=
NM_025220.5:c.1839C>G MANE Select	NP_079496.1:p.Pro613=
NM_153202.4:c.1839C>G	NP_694882.1:p.Pro613=