Canonical Allele Identifier: CA408105031

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652322A>G (hg19) ; chr20:g.3671675A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671675A>G , CM000682.2:g.3671675A>G	GRCh38
NC_000020.10:g.3652322A>G , CM000682.1:g.3652322A>G	GRCh37
NC_000020.9:g.3600322A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1811T>C MANE Select	ENSP00000348912.3:p.Val604Ala
ENST00000350009.6:c.1811T>C	ENSP00000322550.5:p.Val604Ala
ENST00000356518.6:c.1811T>C	ENSP00000348912.2:p.Val604Ala
ENST00000379861.8:c.1811T>C	ENSP00000369190.4:p.Val604Ala
ENST00000466620.5:n.1450T>C
ENST00000617732.1:c.*632-218T>C	ENSP00000483343.1:n.*632-218T>C
ENST00000619289.4:c.1451T>C	ENSP00000484600.1:p.Val484Ala
NM_001282447.1:c.1811T>C	NP_001269376.1:p.Val604Ala
NM_025220.3:c.1811T>C	NP_079496.1:p.Val604Ala
NM_153202.2:c.1811T>C	NP_694882.1:p.Val604Ala
XM_005260843.1:c.1850T>C	XP_005260900.1:p.Val617Ala
XM_006723639.1:c.1850T>C	XP_006723702.1:p.Val617Ala
XM_006723640.1:c.1841T>C	XP_006723703.1:p.Val614Ala
XM_011529366.1:c.1847T>C	XP_011527668.1:p.Val616Ala
XM_011529367.1:c.1808T>C	XP_011527669.1:p.Val603Ala
XM_011529368.1:c.1850T>C	XP_011527670.1:p.Val617Ala
XM_011529369.1:c.1818T>C	XP_011527671.1:p.Ser606=
XM_011529370.1:c.1818T>C	XP_011527672.1:p.Ser606=
XM_011529373.1:c.848T>C	XP_011527675.1:p.Val283Ala
XR_937151.1:n.1954T>C
XR_937152.1:n.1954T>C
XR_937153.1:n.1835T>C
XR_937154.1:n.1835T>C
XR_937155.1:n.1756T>C
XR_937157.1:n.1758T>C
NM_001282447.2:c.1811T>C	NP_001269376.1:p.Val604Ala
NM_025220.4:c.1811T>C	NP_079496.1:p.Val604Ala
NM_153202.3:c.1811T>C	NP_694882.1:p.Val604Ala
XM_011529373.2:c.848T>C	XP_011527675.1:p.Val283Ala
XR_001754405.1:n.1922T>C
XR_002958534.1:n.2031T>C
NM_001282447.3:c.1811T>C	NP_001269376.1:p.Val604Ala
NM_025220.5:c.1811T>C MANE Select	NP_079496.1:p.Val604Ala
NM_153202.4:c.1811T>C	NP_694882.1:p.Val604Ala