Canonical Allele Identifier: CA408103894

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650276T>G (hg19) ; chr20:g.3669629T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669629T>G , CM000682.2:g.3669629T>G	GRCh38
NC_000020.10:g.3650276T>G , CM000682.1:g.3650276T>G	GRCh37
NC_000020.9:g.3598276T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2249A>C MANE Select	ENSP00000348912.3:p.Asp750Ala
ENST00000350009.6:c.2171A>C	ENSP00000322550.5:p.Asp724Ala
ENST00000356518.6:c.2249A>C	ENSP00000348912.2:p.Asp750Ala
ENST00000379861.8:c.2249A>C	ENSP00000369190.4:p.Asp750Ala
ENST00000466620.5:n.1810A>C
ENST00000483362.1:n.997A>C
ENST00000617732.1:c.*936A>C	ENSP00000483343.1:n.*936A>C
ENST00000619289.4:c.1889A>C	ENSP00000484600.1:p.Asp630Ala
NM_001282447.1:c.2249A>C	NP_001269376.1:p.Asp750Ala
NM_025220.3:c.2249A>C	NP_079496.1:p.Asp750Ala
NM_153202.2:c.2171A>C	NP_694882.1:p.Asp724Ala
XM_005260843.1:c.2288A>C	XP_005260900.1:p.Asp763Ala
XM_006723639.1:c.2288A>C	XP_006723702.1:p.Asp763Ala
XM_006723640.1:c.2279A>C	XP_006723703.1:p.Asp760Ala
XM_011529366.1:c.2285A>C	XP_011527668.1:p.Asp762Ala
XM_011529367.1:c.2246A>C	XP_011527669.1:p.Asp749Ala
XM_011529368.1:c.2210A>C	XP_011527670.1:p.Asp737Ala
XM_011529373.1:c.1286A>C	XP_011527675.1:p.Asp429Ala
XR_937151.1:n.2384-259A>C
XR_937152.1:n.2384-259A>C
XR_937153.1:n.2273A>C
XR_937154.1:n.2273A>C
XR_937155.1:n.2194A>C
XR_937157.1:n.2196A>C
NM_001282447.2:c.2249A>C	NP_001269376.1:p.Asp750Ala
NM_025220.4:c.2249A>C	NP_079496.1:p.Asp750Ala
NM_153202.3:c.2171A>C	NP_694882.1:p.Asp724Ala
XM_011529373.2:c.1286A>C	XP_011527675.1:p.Asp429Ala
XR_001754405.1:n.2360A>C
XR_002958534.1:n.2469A>C
NM_001282447.3:c.2249A>C	NP_001269376.1:p.Asp750Ala
NM_025220.5:c.2249A>C MANE Select	NP_079496.1:p.Asp750Ala
NM_153202.4:c.2171A>C	NP_694882.1:p.Asp724Ala