Canonical Allele Identifier: CA408104761

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652110A>G (hg19) ; chr20:g.3671463A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671463A>G , CM000682.2:g.3671463A>G	GRCh38
NC_000020.10:g.3652110A>G , CM000682.1:g.3652110A>G	GRCh37
NC_000020.9:g.3600110A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.1939T>C MANE Select	ENSP00000348912.3:p.Phe647Leu
ENST00000350009.6:c.1906-118T>C	ENSP00000322550.5:n.1906-118T>C
ENST00000356518.6:c.1939T>C	ENSP00000348912.2:p.Phe647Leu
ENST00000379861.8:c.1939T>C	ENSP00000369190.4:p.Phe647Leu
ENST00000466620.5:n.1545-118T>C
ENST00000617732.1:c.*632-6T>C	ENSP00000483343.1:n.*632-6T>C
ENST00000619289.4:c.1579T>C	ENSP00000484600.1:p.Phe527Leu
NM_001282447.1:c.1939T>C	NP_001269376.1:p.Phe647Leu
NM_025220.3:c.1939T>C	NP_079496.1:p.Phe647Leu
NM_153202.2:c.1906-118T>C	NP_694882.1:n.1906-118T>C
XM_005260843.1:c.1978T>C	XP_005260900.1:p.Phe660Leu
XM_006723639.1:c.1978T>C	XP_006723702.1:p.Phe660Leu
XM_006723640.1:c.1969T>C	XP_006723703.1:p.Phe657Leu
XM_011529366.1:c.1975T>C	XP_011527668.1:p.Phe659Leu
XM_011529367.1:c.1936T>C	XP_011527669.1:p.Phe646Leu
XM_011529368.1:c.1945-118T>C	XP_011527670.1:n.1945-118T>C
XM_011529369.1:c.*38T>C	XP_011527671.1:n.*38T>C
XM_011529370.1:c.*5-118T>C	XP_011527672.1:n.*5-118T>C
XM_011529373.1:c.976T>C	XP_011527675.1:p.Phe326Leu
XR_937151.1:n.2082T>C
XR_937152.1:n.2082T>C
XR_937153.1:n.1963T>C
XR_937154.1:n.1963T>C
XR_937155.1:n.1884T>C
XR_937157.1:n.1886T>C
NM_001282447.2:c.1939T>C	NP_001269376.1:p.Phe647Leu
NM_025220.4:c.1939T>C	NP_079496.1:p.Phe647Leu
NM_153202.3:c.1906-118T>C	NP_694882.1:n.1906-118T>C
XM_011529373.2:c.976T>C	XP_011527675.1:p.Phe326Leu
XR_001754405.1:n.2050T>C
XR_002958534.1:n.2159T>C
NM_001282447.3:c.1939T>C	NP_001269376.1:p.Phe647Leu
NM_025220.5:c.1939T>C MANE Select	NP_079496.1:p.Phe647Leu
NM_153202.4:c.1906-118T>C	NP_694882.1:n.1906-118T>C