Canonical Allele Identifier: CA509419177

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649950G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669303G>C , CM000682.2:g.3669303G>C	GRCh38
NC_000020.10:g.3649950G>C , CM000682.1:g.3649950G>C	GRCh37
NC_000020.9:g.3597950G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2400C>G MANE Select	ENSP00000348912.3:p.Pro800=
ENST00000350009.6:c.2322C>G	ENSP00000322550.5:p.Pro774=
ENST00000356518.6:c.2400C>G	ENSP00000348912.2:p.Pro800=
ENST00000379861.8:c.2400C>G	ENSP00000369190.4:p.Pro800=
ENST00000466620.5:n.1961C>G
ENST00000483362.1:n.1323C>G
ENST00000617732.1:c.*1087C>G	ENSP00000483343.1:n.*1087C>G
ENST00000619289.4:c.2040C>G	ENSP00000484600.1:p.Pro680=
NM_001282447.1:c.2400C>G	NP_001269376.1:p.Pro800=
NM_025220.3:c.2400C>G	NP_079496.1:p.Pro800=
NM_153202.2:c.2322C>G	NP_694882.1:p.Pro774=
XM_005260843.1:c.2439C>G	XP_005260900.1:p.Pro813=
XM_006723639.1:c.2439C>G	XP_006723702.1:p.Pro813=
XM_006723640.1:c.2430C>G	XP_006723703.1:p.Pro810=
XM_011529366.1:c.2436C>G	XP_011527668.1:p.Pro812=
XM_011529367.1:c.2397C>G	XP_011527669.1:p.Pro799=
XM_011529368.1:c.2361C>G	XP_011527670.1:p.Pro787=
XM_011529373.1:c.1437C>G	XP_011527675.1:p.Pro479=
XR_937151.1:n.2451C>G
XR_937152.1:n.2451C>G
XR_937153.1:n.2424C>G
XR_937154.1:n.2424C>G
XR_937155.1:n.2345C>G
XR_937157.1:n.2347C>G
NM_001282447.2:c.2400C>G	NP_001269376.1:p.Pro800=
NM_025220.4:c.2400C>G	NP_079496.1:p.Pro800=
NM_153202.3:c.2322C>G	NP_694882.1:p.Pro774=
XM_011529373.2:c.1437C>G	XP_011527675.1:p.Pro479=
XR_001754405.1:n.2511C>G
XR_002958534.1:n.2620C>G
NM_001282447.3:c.2400C>G	NP_001269376.1:p.Pro800=
NM_025220.5:c.2400C>G MANE Select	NP_079496.1:p.Pro800=
NM_153202.4:c.2322C>G	NP_694882.1:p.Pro774=