Canonical Allele Identifier: CA408104656

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652067C>A (hg19) ; chr20:g.3671420C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671420C>A , CM000682.2:g.3671420C>A	GRCh38
NC_000020.10:g.3652067C>A , CM000682.1:g.3652067C>A	GRCh37
NC_000020.9:g.3600067C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1982G>T MANE Select	ENSP00000348912.3:p.Gly661Val
ENST00000350009.6:c.1906-75G>T	ENSP00000322550.5:n.1906-75G>T
ENST00000356518.6:c.1982G>T	ENSP00000348912.2:p.Gly661Val
ENST00000379861.8:c.1982G>T	ENSP00000369190.4:p.Gly661Val
ENST00000466620.5:n.1545-75G>T
ENST00000617732.1:c.*669G>T	ENSP00000483343.1:n.*669G>T
ENST00000619289.4:c.1622G>T	ENSP00000484600.1:p.Gly541Val
NM_001282447.1:c.1982G>T	NP_001269376.1:p.Gly661Val
NM_025220.3:c.1982G>T	NP_079496.1:p.Gly661Val
NM_153202.2:c.1906-75G>T	NP_694882.1:n.1906-75G>T
XM_005260843.1:c.2021G>T	XP_005260900.1:p.Gly674Val
XM_006723639.1:c.2021G>T	XP_006723702.1:p.Gly674Val
XM_006723640.1:c.2012G>T	XP_006723703.1:p.Gly671Val
XM_011529366.1:c.2018G>T	XP_011527668.1:p.Gly673Val
XM_011529367.1:c.1979G>T	XP_011527669.1:p.Gly660Val
XM_011529368.1:c.1945-75G>T	XP_011527670.1:n.1945-75G>T
XM_011529369.1:c.*81G>T	XP_011527671.1:n.*81G>T
XM_011529370.1:c.*5-75G>T	XP_011527672.1:n.*5-75G>T
XM_011529373.1:c.1019G>T	XP_011527675.1:p.Gly340Val
XR_937151.1:n.2125G>T
XR_937152.1:n.2125G>T
XR_937153.1:n.2006G>T
XR_937154.1:n.2006G>T
XR_937155.1:n.1927G>T
XR_937157.1:n.1929G>T
NM_001282447.2:c.1982G>T	NP_001269376.1:p.Gly661Val
NM_025220.4:c.1982G>T	NP_079496.1:p.Gly661Val
NM_153202.3:c.1906-75G>T	NP_694882.1:n.1906-75G>T
XM_011529373.2:c.1019G>T	XP_011527675.1:p.Gly340Val
XR_001754405.1:n.2093G>T
XR_002958534.1:n.2202G>T
NM_001282447.3:c.1982G>T	NP_001269376.1:p.Gly661Val
NM_025220.5:c.1982G>T MANE Select	NP_079496.1:p.Gly661Val
NM_153202.4:c.1906-75G>T	NP_694882.1:n.1906-75G>T