Canonical Allele Identifier: CA408103542

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649970G>A (hg19) ; chr20:g.3669323G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669323G>A , CM000682.2:g.3669323G>A	GRCh38
NC_000020.10:g.3649970G>A , CM000682.1:g.3649970G>A	GRCh37
NC_000020.9:g.3597970G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2380C>T MANE Select	ENSP00000348912.3:p.Pro794Ser
ENST00000350009.6:c.2302C>T	ENSP00000322550.5:p.Pro768Ser
ENST00000356518.6:c.2380C>T	ENSP00000348912.2:p.Pro794Ser
ENST00000379861.8:c.2380C>T	ENSP00000369190.4:p.Pro794Ser
ENST00000466620.5:n.1941C>T
ENST00000483362.1:n.1303C>T
ENST00000617732.1:c.*1067C>T	ENSP00000483343.1:n.*1067C>T
ENST00000619289.4:c.2020C>T	ENSP00000484600.1:p.Pro674Ser
NM_001282447.1:c.2380C>T	NP_001269376.1:p.Pro794Ser
NM_025220.3:c.2380C>T	NP_079496.1:p.Pro794Ser
NM_153202.2:c.2302C>T	NP_694882.1:p.Pro768Ser
XM_005260843.1:c.2419C>T	XP_005260900.1:p.Pro807Ser
XM_006723639.1:c.2419C>T	XP_006723702.1:p.Pro807Ser
XM_006723640.1:c.2410C>T	XP_006723703.1:p.Pro804Ser
XM_011529366.1:c.2416C>T	XP_011527668.1:p.Pro806Ser
XM_011529367.1:c.2377C>T	XP_011527669.1:p.Pro793Ser
XM_011529368.1:c.2341C>T	XP_011527670.1:p.Pro781Ser
XM_011529373.1:c.1417C>T	XP_011527675.1:p.Pro473Ser
XR_937151.1:n.2431C>T
XR_937152.1:n.2431C>T
XR_937153.1:n.2404C>T
XR_937154.1:n.2404C>T
XR_937155.1:n.2325C>T
XR_937157.1:n.2327C>T
NM_001282447.2:c.2380C>T	NP_001269376.1:p.Pro794Ser
NM_025220.4:c.2380C>T	NP_079496.1:p.Pro794Ser
NM_153202.3:c.2302C>T	NP_694882.1:p.Pro768Ser
XM_011529373.2:c.1417C>T	XP_011527675.1:p.Pro473Ser
XR_001754405.1:n.2491C>T
XR_002958534.1:n.2600C>T
NM_001282447.3:c.2380C>T	NP_001269376.1:p.Pro794Ser
NM_025220.5:c.2380C>T MANE Select	NP_079496.1:p.Pro794Ser
NM_153202.4:c.2302C>T	NP_694882.1:p.Pro768Ser