Canonical Allele Identifier: CA2346678887

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671828_3671829delinsCA , CM000682.2:g.3671828_3671829delinsCA	GRCh38
NC_000020.10:g.3652475_3652476delinsCA , CM000682.1:g.3652475_3652476delinsCA	GRCh37
NC_000020.9:g.3600475_3600476delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1706+48_1707-49delinsTG MANE Select	ENSP00000348912.3:n.1706+48_1707-49delinsTG
ENST00000350009.6:c.1706+48_1707-49delinsTG	ENSP00000322550.5:n.1706+48_1707-49delinsTG
ENST00000356518.6:c.1706+48_1707-49delinsTG	ENSP00000348912.2:n.1706+48_1707-49delinsTG
ENST00000379861.8:c.1706+48_1707-49delinsTG	ENSP00000369190.4:n.1706+48_1707-49delinsTG
ENST00000466620.5:n.1345+48_1346-49delinsTG
ENST00000617732.1:c.*632-372_*632-371delinsTG	ENSP00000483343.1:n.*632-372_*632-371delinsTG
ENST00000619289.4:c.1346+48_1347-49delinsTG	ENSP00000484600.1:n.1346+48_1347-49delinsTG
NM_001282447.1:c.1706+48_1707-49delinsTG	NP_001269376.1:n.1706+48_1707-49delinsTG
NM_025220.3:c.1706+48_1707-49delinsTG	NP_079496.1:n.1706+48_1707-49delinsTG
NM_153202.2:c.1706+48_1707-49delinsTG	NP_694882.1:n.1706+48_1707-49delinsTG
XM_005260843.1:c.1745+48_1746-49delinsTG	XP_005260900.1:n.1745+48_1746-49delinsTG
XM_006723639.1:c.1745+48_1746-49delinsTG	XP_006723702.1:n.1745+48_1746-49delinsTG
XM_006723640.1:c.1736+48_1737-49delinsTG	XP_006723703.1:n.1736+48_1737-49delinsTG
XM_011529366.1:c.1742+48_1743-49delinsTG	XP_011527668.1:n.1742+48_1743-49delinsTG
XM_011529367.1:c.1703+48_1704-49delinsTG	XP_011527669.1:n.1703+48_1704-49delinsTG
XM_011529368.1:c.1745+48_1746-49delinsTG	XP_011527670.1:n.1745+48_1746-49delinsTG
XM_011529369.1:c.1713+48_1714-49delinsTG	XP_011527671.1:n.1713+48_1714-49delinsTG
XM_011529370.1:c.1713+48_1714-49delinsTG	XP_011527672.1:n.1713+48_1714-49delinsTG
XM_011529373.1:c.743+48_744-49delinsTG	XP_011527675.1:n.743+48_744-49delinsTG
XR_937151.1:n.1849+48_1850-49delinsTG
XR_937152.1:n.1849+48_1850-49delinsTG
XR_937153.1:n.1730+48_1731-49delinsTG
XR_937154.1:n.1730+48_1731-49delinsTG
XR_937155.1:n.1651+48_1652-49delinsTG
XR_937157.1:n.1653+48_1654-49delinsTG
NM_001282447.2:c.1706+48_1707-49delinsTG	NP_001269376.1:n.1706+48_1707-49delinsTG
NM_025220.4:c.1706+48_1707-49delinsTG	NP_079496.1:n.1706+48_1707-49delinsTG
NM_153202.3:c.1706+48_1707-49delinsTG	NP_694882.1:n.1706+48_1707-49delinsTG
XM_011529373.2:c.743+48_744-49delinsTG	XP_011527675.1:n.743+48_744-49delinsTG
XR_001754405.1:n.1817+48_1818-49delinsTG
XR_002958534.1:n.1926+48_1927-49delinsTG
NM_001282447.3:c.1706+48_1707-49delinsTG	NP_001269376.1:n.1706+48_1707-49delinsTG
NM_025220.5:c.1706+48_1707-49delinsTG MANE Select	NP_079496.1:n.1706+48_1707-49delinsTG
NM_153202.4:c.1706+48_1707-49delinsTG	NP_694882.1:n.1706+48_1707-49delinsTG