Canonical Allele Identifier: CA509419204

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649986G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669339G>A , CM000682.2:g.3669339G>A	GRCh38
NC_000020.10:g.3649986G>A , CM000682.1:g.3649986G>A	GRCh37
NC_000020.9:g.3597986G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2364C>T MANE Select	ENSP00000348912.3:p.His788=
ENST00000350009.6:c.2286C>T	ENSP00000322550.5:p.His762=
ENST00000356518.6:c.2364C>T	ENSP00000348912.2:p.His788=
ENST00000379861.8:c.2364C>T	ENSP00000369190.4:p.His788=
ENST00000466620.5:n.1925C>T
ENST00000483362.1:n.1287C>T
ENST00000617732.1:c.*1051C>T	ENSP00000483343.1:n.*1051C>T
ENST00000619289.4:c.2004C>T	ENSP00000484600.1:p.His668=
NM_001282447.1:c.2364C>T	NP_001269376.1:p.His788=
NM_025220.3:c.2364C>T	NP_079496.1:p.His788=
NM_153202.2:c.2286C>T	NP_694882.1:p.His762=
XM_005260843.1:c.2403C>T	XP_005260900.1:p.His801=
XM_006723639.1:c.2403C>T	XP_006723702.1:p.His801=
XM_006723640.1:c.2394C>T	XP_006723703.1:p.His798=
XM_011529366.1:c.2400C>T	XP_011527668.1:p.His800=
XM_011529367.1:c.2361C>T	XP_011527669.1:p.His787=
XM_011529368.1:c.2325C>T	XP_011527670.1:p.His775=
XM_011529373.1:c.1401C>T	XP_011527675.1:p.His467=
XR_937151.1:n.2415C>T
XR_937152.1:n.2415C>T
XR_937153.1:n.2388C>T
XR_937154.1:n.2388C>T
XR_937155.1:n.2309C>T
XR_937157.1:n.2311C>T
NM_001282447.2:c.2364C>T	NP_001269376.1:p.His788=
NM_025220.4:c.2364C>T	NP_079496.1:p.His788=
NM_153202.3:c.2286C>T	NP_694882.1:p.His762=
XM_011529373.2:c.1401C>T	XP_011527675.1:p.His467=
XR_001754405.1:n.2475C>T
XR_002958534.1:n.2584C>T
NM_001282447.3:c.2364C>T	NP_001269376.1:p.His788=
NM_025220.5:c.2364C>T MANE Select	NP_079496.1:p.His788=
NM_153202.4:c.2286C>T	NP_694882.1:p.His762=