Canonical Allele Identifier: CA408105364

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652572C>G (hg19) ; chr20:g.3671925C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671925C>G , CM000682.2:g.3671925C>G	GRCh38
NC_000020.10:g.3652572C>G , CM000682.1:g.3652572C>G	GRCh37
NC_000020.9:g.3600572C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1658G>C MANE Select	ENSP00000348912.3:p.Gly553Ala
ENST00000350009.6:c.1658G>C	ENSP00000322550.5:p.Gly553Ala
ENST00000356518.6:c.1658G>C	ENSP00000348912.2:p.Gly553Ala
ENST00000379861.8:c.1658G>C	ENSP00000369190.4:p.Gly553Ala
ENST00000466620.5:n.1297G>C
ENST00000617732.1:c.*632-468G>C	ENSP00000483343.1:n.*632-468G>C
ENST00000619289.4:c.1298G>C	ENSP00000484600.1:p.Gly433Ala
NM_001282447.1:c.1658G>C	NP_001269376.1:p.Gly553Ala
NM_025220.3:c.1658G>C	NP_079496.1:p.Gly553Ala
NM_153202.2:c.1658G>C	NP_694882.1:p.Gly553Ala
XM_005260843.1:c.1697G>C	XP_005260900.1:p.Gly566Ala
XM_006723639.1:c.1697G>C	XP_006723702.1:p.Gly566Ala
XM_006723640.1:c.1688G>C	XP_006723703.1:p.Gly563Ala
XM_011529366.1:c.1694G>C	XP_011527668.1:p.Gly565Ala
XM_011529367.1:c.1655G>C	XP_011527669.1:p.Gly552Ala
XM_011529368.1:c.1697G>C	XP_011527670.1:p.Gly566Ala
XM_011529369.1:c.1665G>C	XP_011527671.1:p.Trp555Cys
XM_011529370.1:c.1665G>C	XP_011527672.1:p.Trp555Cys
XM_011529373.1:c.695G>C	XP_011527675.1:p.Gly232Ala
XR_937151.1:n.1801G>C
XR_937152.1:n.1801G>C
XR_937153.1:n.1682G>C
XR_937154.1:n.1682G>C
XR_937155.1:n.1603G>C
XR_937157.1:n.1605G>C
NM_001282447.2:c.1658G>C	NP_001269376.1:p.Gly553Ala
NM_025220.4:c.1658G>C	NP_079496.1:p.Gly553Ala
NM_153202.3:c.1658G>C	NP_694882.1:p.Gly553Ala
XM_011529373.2:c.695G>C	XP_011527675.1:p.Gly232Ala
XR_001754405.1:n.1769G>C
XR_002958534.1:n.1878G>C
NM_001282447.3:c.1658G>C	NP_001269376.1:p.Gly553Ala
NM_025220.5:c.1658G>C MANE Select	NP_079496.1:p.Gly553Ala
NM_153202.4:c.1658G>C	NP_694882.1:p.Gly553Ala