Canonical Allele Identifier: CA509419250
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3669589G>C , CM000682.2:g.3669589G>C GRCh38
NC_000020.10:g.3650236G>C , CM000682.1:g.3650236G>C GRCh37
NC_000020.9:g.3598236G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2289C>G MANE Select ENSP00000348912.3:p.Pro763=
ENST00000350009.6:c.2211C>G ENSP00000322550.5:p.Pro737=
ENST00000356518.6:c.2289C>G ENSP00000348912.2:p.Pro763=
ENST00000379861.8:c.2289C>G ENSP00000369190.4:p.Pro763=
ENST00000466620.5:n.1850C>G
ENST00000483362.1:n.1037C>G
ENST00000617732.1:c.*976C>G ENSP00000483343.1:n.*976C>G
ENST00000619289.4:c.1929C>G ENSP00000484600.1:p.Pro643=
NM_001282447.1:c.2289C>G NP_001269376.1:p.Pro763=
NM_025220.3:c.2289C>G NP_079496.1:p.Pro763=
NM_153202.2:c.2211C>G NP_694882.1:p.Pro737=
XM_005260843.1:c.2328C>G XP_005260900.1:p.Pro776=
XM_006723639.1:c.2328C>G XP_006723702.1:p.Pro776=
XM_006723640.1:c.2319C>G XP_006723703.1:p.Pro773=
XM_011529366.1:c.2325C>G XP_011527668.1:p.Pro775=
XM_011529367.1:c.2286C>G XP_011527669.1:p.Pro762=
XM_011529368.1:c.2250C>G XP_011527670.1:p.Pro750=
XM_011529373.1:c.1326C>G XP_011527675.1:p.Pro442=
XR_937151.1:n.2384-219C>G
XR_937152.1:n.2384-219C>G
XR_937153.1:n.2313C>G
XR_937154.1:n.2313C>G
XR_937155.1:n.2234C>G
XR_937157.1:n.2236C>G
NM_001282447.2:c.2289C>G NP_001269376.1:p.Pro763=
NM_025220.4:c.2289C>G NP_079496.1:p.Pro763=
NM_153202.3:c.2211C>G NP_694882.1:p.Pro737=
XM_011529373.2:c.1326C>G XP_011527675.1:p.Pro442=
XR_001754405.1:n.2400C>G
XR_002958534.1:n.2509C>G
NM_001282447.3:c.2289C>G NP_001269376.1:p.Pro763=
NM_025220.5:c.2289C>G MANE Select NP_079496.1:p.Pro763=
NM_153202.4:c.2211C>G NP_694882.1:p.Pro737=