Canonical Allele Identifier: CA2815081893

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671838_3671839insAACA , CM000682.2:g.3671838_3671839insAACA	GRCh38
NC_000020.10:g.3652485_3652486insAACA , CM000682.1:g.3652485_3652486insAACA	GRCh37
NC_000020.9:g.3600485_3600486insAACA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1706+38_1706+39insTGTT MANE Select	ENSP00000348912.3:n.1706+38_1706+39insTGTT
ENST00000350009.6:c.1706+38_1706+39insTGTT	ENSP00000322550.5:n.1706+38_1706+39insTGTT
ENST00000356518.6:c.1706+38_1706+39insTGTT	ENSP00000348912.2:n.1706+38_1706+39insTGTT
ENST00000379861.8:c.1706+38_1706+39insTGTT	ENSP00000369190.4:n.1706+38_1706+39insTGTT
ENST00000466620.5:n.1345+38_1345+39insTGTT
ENST00000617732.1:c.*632-382_*632-381insTGTT	ENSP00000483343.1:n.*632-382_*632-381insTGTT
ENST00000619289.4:c.1346+38_1346+39insTGTT	ENSP00000484600.1:n.1346+38_1346+39insTGTT
NM_001282447.1:c.1706+38_1706+39insTGTT	NP_001269376.1:n.1706+38_1706+39insTGTT
NM_025220.3:c.1706+38_1706+39insTGTT	NP_079496.1:n.1706+38_1706+39insTGTT
NM_153202.2:c.1706+38_1706+39insTGTT	NP_694882.1:n.1706+38_1706+39insTGTT
XM_005260843.1:c.1745+38_1745+39insTGTT	XP_005260900.1:n.1745+38_1745+39insTGTT
XM_006723639.1:c.1745+38_1745+39insTGTT	XP_006723702.1:n.1745+38_1745+39insTGTT
XM_006723640.1:c.1736+38_1736+39insTGTT	XP_006723703.1:n.1736+38_1736+39insTGTT
XM_011529366.1:c.1742+38_1742+39insTGTT	XP_011527668.1:n.1742+38_1742+39insTGTT
XM_011529367.1:c.1703+38_1703+39insTGTT	XP_011527669.1:n.1703+38_1703+39insTGTT
XM_011529368.1:c.1745+38_1745+39insTGTT	XP_011527670.1:n.1745+38_1745+39insTGTT
XM_011529369.1:c.1713+38_1713+39insTGTT	XP_011527671.1:n.1713+38_1713+39insTGTT
XM_011529370.1:c.1713+38_1713+39insTGTT	XP_011527672.1:n.1713+38_1713+39insTGTT
XM_011529373.1:c.743+38_743+39insTGTT	XP_011527675.1:n.743+38_743+39insTGTT
XR_937151.1:n.1849+38_1849+39insTGTT
XR_937152.1:n.1849+38_1849+39insTGTT
XR_937153.1:n.1730+38_1730+39insTGTT
XR_937154.1:n.1730+38_1730+39insTGTT
XR_937155.1:n.1651+38_1651+39insTGTT
XR_937157.1:n.1653+38_1653+39insTGTT
NM_001282447.2:c.1706+38_1706+39insTGTT	NP_001269376.1:n.1706+38_1706+39insTGTT
NM_025220.4:c.1706+38_1706+39insTGTT	NP_079496.1:n.1706+38_1706+39insTGTT
NM_153202.3:c.1706+38_1706+39insTGTT	NP_694882.1:n.1706+38_1706+39insTGTT
XM_011529373.2:c.743+38_743+39insTGTT	XP_011527675.1:n.743+38_743+39insTGTT
XR_001754405.1:n.1817+38_1817+39insTGTT
XR_002958534.1:n.1926+38_1926+39insTGTT
NM_001282447.3:c.1706+38_1706+39insTGTT	NP_001269376.1:n.1706+38_1706+39insTGTT
NM_025220.5:c.1706+38_1706+39insTGTT MANE Select	NP_079496.1:n.1706+38_1706+39insTGTT
NM_153202.4:c.1706+38_1706+39insTGTT	NP_694882.1:n.1706+38_1706+39insTGTT