Canonical Allele Identifier: CA408104728

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652097T>G (hg19) ; chr20:g.3671450T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671450T>G , CM000682.2:g.3671450T>G	GRCh38
NC_000020.10:g.3652097T>G , CM000682.1:g.3652097T>G	GRCh37
NC_000020.9:g.3600097T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1952A>C MANE Select	ENSP00000348912.3:p.Gln651Pro
ENST00000350009.6:c.1906-105A>C	ENSP00000322550.5:n.1906-105A>C
ENST00000356518.6:c.1952A>C	ENSP00000348912.2:p.Gln651Pro
ENST00000379861.8:c.1952A>C	ENSP00000369190.4:p.Gln651Pro
ENST00000466620.5:n.1545-105A>C
ENST00000617732.1:c.*639A>C	ENSP00000483343.1:n.*639A>C
ENST00000619289.4:c.1592A>C	ENSP00000484600.1:p.Gln531Pro
NM_001282447.1:c.1952A>C	NP_001269376.1:p.Gln651Pro
NM_025220.3:c.1952A>C	NP_079496.1:p.Gln651Pro
NM_153202.2:c.1906-105A>C	NP_694882.1:n.1906-105A>C
XM_005260843.1:c.1991A>C	XP_005260900.1:p.Gln664Pro
XM_006723639.1:c.1991A>C	XP_006723702.1:p.Gln664Pro
XM_006723640.1:c.1982A>C	XP_006723703.1:p.Gln661Pro
XM_011529366.1:c.1988A>C	XP_011527668.1:p.Gln663Pro
XM_011529367.1:c.1949A>C	XP_011527669.1:p.Gln650Pro
XM_011529368.1:c.1945-105A>C	XP_011527670.1:n.1945-105A>C
XM_011529369.1:c.*51A>C	XP_011527671.1:n.*51A>C
XM_011529370.1:c.*5-105A>C	XP_011527672.1:n.*5-105A>C
XM_011529373.1:c.989A>C	XP_011527675.1:p.Gln330Pro
XR_937151.1:n.2095A>C
XR_937152.1:n.2095A>C
XR_937153.1:n.1976A>C
XR_937154.1:n.1976A>C
XR_937155.1:n.1897A>C
XR_937157.1:n.1899A>C
NM_001282447.2:c.1952A>C	NP_001269376.1:p.Gln651Pro
NM_025220.4:c.1952A>C	NP_079496.1:p.Gln651Pro
NM_153202.3:c.1906-105A>C	NP_694882.1:n.1906-105A>C
XM_011529373.2:c.989A>C	XP_011527675.1:p.Gln330Pro
XR_001754405.1:n.2063A>C
XR_002958534.1:n.2172A>C
NM_001282447.3:c.1952A>C	NP_001269376.1:p.Gln651Pro
NM_025220.5:c.1952A>C MANE Select	NP_079496.1:p.Gln651Pro
NM_153202.4:c.1906-105A>C	NP_694882.1:n.1906-105A>C