Canonical Allele Identifier: CA408103397
Gene: ADAM33 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3668964C>G , CM000682.2:g.3668964C>G GRCh38
NC_000020.10:g.3649611C>G , CM000682.1:g.3649611C>G GRCh37
NC_000020.9:g.3597611C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000356518.7:c.2441G>C MANE Select ENSP00000348912.3:p.Ter814Ser
ENST00000350009.6:c.2363G>C ENSP00000322550.5:p.Ter788Ser
ENST00000356518.6:c.2441G>C ENSP00000348912.2:p.Ter814Ser
ENST00000379861.8:c.2438G>C ENSP00000369190.4:p.Ter813Ser
ENST00000466620.5:n.2002G>C
ENST00000483362.1:n.1364G>C
ENST00000617732.1:c.*1125G>C ENSP00000483343.1:n.*1125G>C
ENST00000619289.4:c.2078G>C ENSP00000484600.1:p.Ter693Ser
NM_001282447.1:c.2438G>C NP_001269376.1:p.Ter813Ser
NM_025220.3:c.2441G>C NP_079496.1:p.Ter814Ser
NM_153202.2:c.2363G>C NP_694882.1:p.Ter788Ser
XM_005260843.1:c.2480G>C XP_005260900.1:p.Ter827Ser
XM_006723639.1:c.2477G>C XP_006723702.1:p.Ter826Ser
XM_006723640.1:c.2471G>C XP_006723703.1:p.Ter824Ser
XM_011529366.1:c.2477G>C XP_011527668.1:p.Ter826Ser
XM_011529367.1:c.2438G>C XP_011527669.1:p.Ter813Ser
XM_011529368.1:c.2402G>C XP_011527670.1:p.Ter801Ser
XM_011529373.1:c.1478G>C XP_011527675.1:p.Ter493Ser
XR_937153.1:n.2462G>C
XR_937154.1:n.2462G>C
XR_937155.1:n.2383G>C
XR_937157.1:n.2385G>C
NM_001282447.2:c.2438G>C NP_001269376.1:p.Ter813Ser
NM_025220.4:c.2441G>C NP_079496.1:p.Ter814Ser
NM_153202.3:c.2363G>C NP_694882.1:p.Ter788Ser
XM_011529373.2:c.1478G>C XP_011527675.1:p.Ter493Ser
XR_001754405.1:n.2549G>C
XR_002958534.1:n.2658G>C
NM_001282447.3:c.2438G>C NP_001269376.1:p.Ter813Ser
NM_025220.5:c.2441G>C MANE Select NP_079496.1:p.Ter814Ser
NM_153202.4:c.2363G>C NP_694882.1:p.Ter788Ser