Canonical Allele Identifier: CA408103449

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649633T>C (hg19) ; chr20:g.3668986T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668986T>C , CM000682.2:g.3668986T>C	GRCh38
NC_000020.10:g.3649633T>C , CM000682.1:g.3649633T>C	GRCh37
NC_000020.9:g.3597633T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2419A>G MANE Select	ENSP00000348912.3:p.Met807Val
ENST00000350009.6:c.2341A>G	ENSP00000322550.5:p.Met781Val
ENST00000356518.6:c.2419A>G	ENSP00000348912.2:p.Met807Val
ENST00000379861.8:c.2416A>G	ENSP00000369190.4:p.Met806Val
ENST00000466620.5:n.1980A>G
ENST00000483362.1:n.1342A>G
ENST00000617732.1:c.*1103A>G	ENSP00000483343.1:n.*1103A>G
ENST00000619289.4:c.2056A>G	ENSP00000484600.1:p.Met686Val
NM_001282447.1:c.2416A>G	NP_001269376.1:p.Met806Val
NM_025220.3:c.2419A>G	NP_079496.1:p.Met807Val
NM_153202.2:c.2341A>G	NP_694882.1:p.Met781Val
XM_005260843.1:c.2458A>G	XP_005260900.1:p.Met820Val
XM_006723639.1:c.2455A>G	XP_006723702.1:p.Met819Val
XM_006723640.1:c.2449A>G	XP_006723703.1:p.Met817Val
XM_011529366.1:c.2455A>G	XP_011527668.1:p.Met819Val
XM_011529367.1:c.2416A>G	XP_011527669.1:p.Met806Val
XM_011529368.1:c.2380A>G	XP_011527670.1:p.Met794Val
XM_011529373.1:c.1456A>G	XP_011527675.1:p.Met486Val
XR_937151.1:n.2470A>G
XR_937152.1:n.2467A>G
XR_937153.1:n.2440A>G
XR_937154.1:n.2440A>G
XR_937155.1:n.2361A>G
XR_937157.1:n.2363A>G
NM_001282447.2:c.2416A>G	NP_001269376.1:p.Met806Val
NM_025220.4:c.2419A>G	NP_079496.1:p.Met807Val
NM_153202.3:c.2341A>G	NP_694882.1:p.Met781Val
XM_011529373.2:c.1456A>G	XP_011527675.1:p.Met486Val
XR_001754405.1:n.2527A>G
XR_002958534.1:n.2636A>G
NM_001282447.3:c.2416A>G	NP_001269376.1:p.Met806Val
NM_025220.5:c.2419A>G MANE Select	NP_079496.1:p.Met807Val
NM_153202.4:c.2341A>G	NP_694882.1:p.Met781Val