Canonical Allele Identifier: CA408103781

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650223G>C (hg19) ; chr20:g.3669576G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669576G>C , CM000682.2:g.3669576G>C	GRCh38
NC_000020.10:g.3650223G>C , CM000682.1:g.3650223G>C	GRCh37
NC_000020.9:g.3598223G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2302C>G MANE Select	ENSP00000348912.3:p.Pro768Ala
ENST00000350009.6:c.2224C>G	ENSP00000322550.5:p.Pro742Ala
ENST00000356518.6:c.2302C>G	ENSP00000348912.2:p.Pro768Ala
ENST00000379861.8:c.2302C>G	ENSP00000369190.4:p.Pro768Ala
ENST00000466620.5:n.1863C>G
ENST00000483362.1:n.1050C>G
ENST00000617732.1:c.*989C>G	ENSP00000483343.1:n.*989C>G
ENST00000619289.4:c.1942C>G	ENSP00000484600.1:p.Pro648Ala
NM_001282447.1:c.2302C>G	NP_001269376.1:p.Pro768Ala
NM_025220.3:c.2302C>G	NP_079496.1:p.Pro768Ala
NM_153202.2:c.2224C>G	NP_694882.1:p.Pro742Ala
XM_005260843.1:c.2341C>G	XP_005260900.1:p.Pro781Ala
XM_006723639.1:c.2341C>G	XP_006723702.1:p.Pro781Ala
XM_006723640.1:c.2332C>G	XP_006723703.1:p.Pro778Ala
XM_011529366.1:c.2338C>G	XP_011527668.1:p.Pro780Ala
XM_011529367.1:c.2299C>G	XP_011527669.1:p.Pro767Ala
XM_011529368.1:c.2263C>G	XP_011527670.1:p.Pro755Ala
XM_011529373.1:c.1339C>G	XP_011527675.1:p.Pro447Ala
XR_937151.1:n.2384-206C>G
XR_937152.1:n.2384-206C>G
XR_937153.1:n.2326C>G
XR_937154.1:n.2326C>G
XR_937155.1:n.2247C>G
XR_937157.1:n.2249C>G
NM_001282447.2:c.2302C>G	NP_001269376.1:p.Pro768Ala
NM_025220.4:c.2302C>G	NP_079496.1:p.Pro768Ala
NM_153202.3:c.2224C>G	NP_694882.1:p.Pro742Ala
XM_011529373.2:c.1339C>G	XP_011527675.1:p.Pro447Ala
XR_001754405.1:n.2413C>G
XR_002958534.1:n.2522C>G
NM_001282447.3:c.2302C>G	NP_001269376.1:p.Pro768Ala
NM_025220.5:c.2302C>G MANE Select	NP_079496.1:p.Pro768Ala
NM_153202.4:c.2224C>G	NP_694882.1:p.Pro742Ala