Canonical Allele Identifier: CA509419199

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649974A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669327A>G , CM000682.2:g.3669327A>G	GRCh38
NC_000020.10:g.3649974A>G , CM000682.1:g.3649974A>G	GRCh37
NC_000020.9:g.3597974A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2376T>C MANE Select	ENSP00000348912.3:p.Pro792=
ENST00000350009.6:c.2298T>C	ENSP00000322550.5:p.Pro766=
ENST00000356518.6:c.2376T>C	ENSP00000348912.2:p.Pro792=
ENST00000379861.8:c.2376T>C	ENSP00000369190.4:p.Pro792=
ENST00000466620.5:n.1937T>C
ENST00000483362.1:n.1299T>C
ENST00000617732.1:c.*1063T>C	ENSP00000483343.1:n.*1063T>C
ENST00000619289.4:c.2016T>C	ENSP00000484600.1:p.Pro672=
NM_001282447.1:c.2376T>C	NP_001269376.1:p.Pro792=
NM_025220.3:c.2376T>C	NP_079496.1:p.Pro792=
NM_153202.2:c.2298T>C	NP_694882.1:p.Pro766=
XM_005260843.1:c.2415T>C	XP_005260900.1:p.Pro805=
XM_006723639.1:c.2415T>C	XP_006723702.1:p.Pro805=
XM_006723640.1:c.2406T>C	XP_006723703.1:p.Pro802=
XM_011529366.1:c.2412T>C	XP_011527668.1:p.Pro804=
XM_011529367.1:c.2373T>C	XP_011527669.1:p.Pro791=
XM_011529368.1:c.2337T>C	XP_011527670.1:p.Pro779=
XM_011529373.1:c.1413T>C	XP_011527675.1:p.Pro471=
XR_937151.1:n.2427T>C
XR_937152.1:n.2427T>C
XR_937153.1:n.2400T>C
XR_937154.1:n.2400T>C
XR_937155.1:n.2321T>C
XR_937157.1:n.2323T>C
NM_001282447.2:c.2376T>C	NP_001269376.1:p.Pro792=
NM_025220.4:c.2376T>C	NP_079496.1:p.Pro792=
NM_153202.3:c.2298T>C	NP_694882.1:p.Pro766=
XM_011529373.2:c.1413T>C	XP_011527675.1:p.Pro471=
XR_001754405.1:n.2487T>C
XR_002958534.1:n.2596T>C
NM_001282447.3:c.2376T>C	NP_001269376.1:p.Pro792=
NM_025220.5:c.2376T>C MANE Select	NP_079496.1:p.Pro792=
NM_153202.4:c.2298T>C	NP_694882.1:p.Pro766=