Canonical Allele Identifier: CA509419246

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650227C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669580C>T , CM000682.2:g.3669580C>T	GRCh38
NC_000020.10:g.3650227C>T , CM000682.1:g.3650227C>T	GRCh37
NC_000020.9:g.3598227C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2298G>A MANE Select	ENSP00000348912.3:p.Leu766=
ENST00000350009.6:c.2220G>A	ENSP00000322550.5:p.Leu740=
ENST00000356518.6:c.2298G>A	ENSP00000348912.2:p.Leu766=
ENST00000379861.8:c.2298G>A	ENSP00000369190.4:p.Leu766=
ENST00000466620.5:n.1859G>A
ENST00000483362.1:n.1046G>A
ENST00000617732.1:c.*985G>A	ENSP00000483343.1:n.*985G>A
ENST00000619289.4:c.1938G>A	ENSP00000484600.1:p.Leu646=
NM_001282447.1:c.2298G>A	NP_001269376.1:p.Leu766=
NM_025220.3:c.2298G>A	NP_079496.1:p.Leu766=
NM_153202.2:c.2220G>A	NP_694882.1:p.Leu740=
XM_005260843.1:c.2337G>A	XP_005260900.1:p.Leu779=
XM_006723639.1:c.2337G>A	XP_006723702.1:p.Leu779=
XM_006723640.1:c.2328G>A	XP_006723703.1:p.Leu776=
XM_011529366.1:c.2334G>A	XP_011527668.1:p.Leu778=
XM_011529367.1:c.2295G>A	XP_011527669.1:p.Leu765=
XM_011529368.1:c.2259G>A	XP_011527670.1:p.Leu753=
XM_011529373.1:c.1335G>A	XP_011527675.1:p.Leu445=
XR_937151.1:n.2384-210G>A
XR_937152.1:n.2384-210G>A
XR_937153.1:n.2322G>A
XR_937154.1:n.2322G>A
XR_937155.1:n.2243G>A
XR_937157.1:n.2245G>A
NM_001282447.2:c.2298G>A	NP_001269376.1:p.Leu766=
NM_025220.4:c.2298G>A	NP_079496.1:p.Leu766=
NM_153202.3:c.2220G>A	NP_694882.1:p.Leu740=
XM_011529373.2:c.1335G>A	XP_011527675.1:p.Leu445=
XR_001754405.1:n.2409G>A
XR_002958534.1:n.2518G>A
NM_001282447.3:c.2298G>A	NP_001269376.1:p.Leu766=
NM_025220.5:c.2298G>A MANE Select	NP_079496.1:p.Leu766=
NM_153202.4:c.2220G>A	NP_694882.1:p.Leu740=