Canonical Allele Identifier: CA408103553

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649976G>T (hg19) ; chr20:g.3669329G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669329G>T , CM000682.2:g.3669329G>T	GRCh38
NC_000020.10:g.3649976G>T , CM000682.1:g.3649976G>T	GRCh37
NC_000020.9:g.3597976G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2374C>A MANE Select	ENSP00000348912.3:p.Pro792Thr
ENST00000350009.6:c.2296C>A	ENSP00000322550.5:p.Pro766Thr
ENST00000356518.6:c.2374C>A	ENSP00000348912.2:p.Pro792Thr
ENST00000379861.8:c.2374C>A	ENSP00000369190.4:p.Pro792Thr
ENST00000466620.5:n.1935C>A
ENST00000483362.1:n.1297C>A
ENST00000617732.1:c.*1061C>A	ENSP00000483343.1:n.*1061C>A
ENST00000619289.4:c.2014C>A	ENSP00000484600.1:p.Pro672Thr
NM_001282447.1:c.2374C>A	NP_001269376.1:p.Pro792Thr
NM_025220.3:c.2374C>A	NP_079496.1:p.Pro792Thr
NM_153202.2:c.2296C>A	NP_694882.1:p.Pro766Thr
XM_005260843.1:c.2413C>A	XP_005260900.1:p.Pro805Thr
XM_006723639.1:c.2413C>A	XP_006723702.1:p.Pro805Thr
XM_006723640.1:c.2404C>A	XP_006723703.1:p.Pro802Thr
XM_011529366.1:c.2410C>A	XP_011527668.1:p.Pro804Thr
XM_011529367.1:c.2371C>A	XP_011527669.1:p.Pro791Thr
XM_011529368.1:c.2335C>A	XP_011527670.1:p.Pro779Thr
XM_011529373.1:c.1411C>A	XP_011527675.1:p.Pro471Thr
XR_937151.1:n.2425C>A
XR_937152.1:n.2425C>A
XR_937153.1:n.2398C>A
XR_937154.1:n.2398C>A
XR_937155.1:n.2319C>A
XR_937157.1:n.2321C>A
NM_001282447.2:c.2374C>A	NP_001269376.1:p.Pro792Thr
NM_025220.4:c.2374C>A	NP_079496.1:p.Pro792Thr
NM_153202.3:c.2296C>A	NP_694882.1:p.Pro766Thr
XM_011529373.2:c.1411C>A	XP_011527675.1:p.Pro471Thr
XR_001754405.1:n.2485C>A
XR_002958534.1:n.2594C>A
NM_001282447.3:c.2374C>A	NP_001269376.1:p.Pro792Thr
NM_025220.5:c.2374C>A MANE Select	NP_079496.1:p.Pro792Thr
NM_153202.4:c.2296C>A	NP_694882.1:p.Pro766Thr