Canonical Allele Identifier: CA2346678674
Gene: ADAM33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3671446_3671447delinsGC , CM000682.2:g.3671446_3671447delinsGC GRCh38
NC_000020.10:g.3652093_3652094delinsGC , CM000682.1:g.3652093_3652094delinsGC GRCh37
NC_000020.9:g.3600093_3600094delinsGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356518.7:c.1955_1956delinsGC MANE Select ENSP00000348912.3:p.Arg652=
ENST00000350009.6:c.1906-102_1906-101delinsGC ENSP00000322550.5:n.1906-102_1906-101delinsGC
ENST00000356518.6:c.1955_1956delinsGC ENSP00000348912.2:p.Arg652=
ENST00000379861.8:c.1955_1956delinsGC ENSP00000369190.4:p.Arg652=
ENST00000466620.5:n.1545-102_1545-101delinsGC
ENST00000617732.1:c.*642_*643delinsGC ENSP00000483343.1:n.*642_*643delinsGC
ENST00000619289.4:c.1595_1596delinsGC ENSP00000484600.1:p.Arg532=
NM_001282447.1:c.1955_1956delinsGC NP_001269376.1:p.Arg652=
NM_025220.3:c.1955_1956delinsGC NP_079496.1:p.Arg652=
NM_153202.2:c.1906-102_1906-101delinsGC NP_694882.1:n.1906-102_1906-101delinsGC
XM_005260843.1:c.1994_1995delinsGC XP_005260900.1:p.Arg665=
XM_006723639.1:c.1994_1995delinsGC XP_006723702.1:p.Arg665=
XM_006723640.1:c.1985_1986delinsGC XP_006723703.1:p.Arg662=
XM_011529366.1:c.1991_1992delinsGC XP_011527668.1:p.Arg664=
XM_011529367.1:c.1952_1953delinsGC XP_011527669.1:p.Arg651=
XM_011529368.1:c.1945-102_1945-101delinsGC XP_011527670.1:n.1945-102_1945-101delinsGC
XM_011529369.1:c.*54_*55delinsGC XP_011527671.1:n.*54_*55delinsGC
XM_011529370.1:c.*5-102_*5-101delinsGC XP_011527672.1:n.*5-102_*5-101delinsGC
XM_011529373.1:c.992_993delinsGC XP_011527675.1:p.Arg331=
XR_937151.1:n.2098_2099delinsGC
XR_937152.1:n.2098_2099delinsGC
XR_937153.1:n.1979_1980delinsGC
XR_937154.1:n.1979_1980delinsGC
XR_937155.1:n.1900_1901delinsGC
XR_937157.1:n.1902_1903delinsGC
NM_001282447.2:c.1955_1956delinsGC NP_001269376.1:p.Arg652=
NM_025220.4:c.1955_1956delinsGC NP_079496.1:p.Arg652=
NM_153202.3:c.1906-102_1906-101delinsGC NP_694882.1:n.1906-102_1906-101delinsGC
XM_011529373.2:c.992_993delinsGC XP_011527675.1:p.Arg331=
XR_001754405.1:n.2066_2067delinsGC
XR_002958534.1:n.2175_2176delinsGC
NM_001282447.3:c.1955_1956delinsGC NP_001269376.1:p.Arg652=
NM_025220.5:c.1955_1956delinsGC MANE Select NP_079496.1:p.Arg652=
NM_153202.4:c.1906-102_1906-101delinsGC NP_694882.1:n.1906-102_1906-101delinsGC