Canonical Allele Identifier: CA509419188

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649965T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669318T>A , CM000682.2:g.3669318T>A	GRCh38
NC_000020.10:g.3649965T>A , CM000682.1:g.3649965T>A	GRCh37
NC_000020.9:g.3597965T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2385A>T MANE Select	ENSP00000348912.3:p.Ala795=
ENST00000350009.6:c.2307A>T	ENSP00000322550.5:p.Ala769=
ENST00000356518.6:c.2385A>T	ENSP00000348912.2:p.Ala795=
ENST00000379861.8:c.2385A>T	ENSP00000369190.4:p.Ala795=
ENST00000466620.5:n.1946A>T
ENST00000483362.1:n.1308A>T
ENST00000617732.1:c.*1072A>T	ENSP00000483343.1:n.*1072A>T
ENST00000619289.4:c.2025A>T	ENSP00000484600.1:p.Ala675=
NM_001282447.1:c.2385A>T	NP_001269376.1:p.Ala795=
NM_025220.3:c.2385A>T	NP_079496.1:p.Ala795=
NM_153202.2:c.2307A>T	NP_694882.1:p.Ala769=
XM_005260843.1:c.2424A>T	XP_005260900.1:p.Ala808=
XM_006723639.1:c.2424A>T	XP_006723702.1:p.Ala808=
XM_006723640.1:c.2415A>T	XP_006723703.1:p.Ala805=
XM_011529366.1:c.2421A>T	XP_011527668.1:p.Ala807=
XM_011529367.1:c.2382A>T	XP_011527669.1:p.Ala794=
XM_011529368.1:c.2346A>T	XP_011527670.1:p.Ala782=
XM_011529373.1:c.1422A>T	XP_011527675.1:p.Ala474=
XR_937151.1:n.2436A>T
XR_937152.1:n.2436A>T
XR_937153.1:n.2409A>T
XR_937154.1:n.2409A>T
XR_937155.1:n.2330A>T
XR_937157.1:n.2332A>T
NM_001282447.2:c.2385A>T	NP_001269376.1:p.Ala795=
NM_025220.4:c.2385A>T	NP_079496.1:p.Ala795=
NM_153202.3:c.2307A>T	NP_694882.1:p.Ala769=
XM_011529373.2:c.1422A>T	XP_011527675.1:p.Ala474=
XR_001754405.1:n.2496A>T
XR_002958534.1:n.2605A>T
NM_001282447.3:c.2385A>T	NP_001269376.1:p.Ala795=
NM_025220.5:c.2385A>T MANE Select	NP_079496.1:p.Ala795=
NM_153202.4:c.2307A>T	NP_694882.1:p.Ala769=