Canonical Allele Identifier: CA8703072

Gene: STRADA

Linked Data

• ClinVar Variation Id: 536753
• ClinVar RCV Id: RCV000645399
• dbSNP Id: rs751571199
• ExAC: 17:61781101 C / T
• gnomAD v2: 17-61781101-C-T
• gnomAD v3: 17-63703741-C-T
• gnomAD v4: 17-63703741-C-T
• MyVariant Identifiers: chr17:g.61781101C>T (hg19) ; chr17:g.63703741C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63703741C>T , CM000679.2:g.63703741C>T	GRCh38
NC_000017.10:g.61781101C>T , CM000679.1:g.61781101C>T	GRCh37
NC_000017.9:g.59134833C>T	NCBI36
NG_015817.1:g.43230G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000245865.10:c.*1138G>A	ENSP00000245865.5:n.*1138G>A
ENST00000336174.12:c.1154G>A MANE Select	ENSP00000336655.6:p.Arg385His
ENST00000375840.9:c.980G>A	ENSP00000365000.4:p.Arg327His
ENST00000392950.9:c.*542G>A	ENSP00000376677.4:n.*542G>A
ENST00000447001.8:c.*31G>A	ENSP00000398841.3:n.*31G>A
ENST00000580039.6:c.957G>A
ENST00000582026.2:c.422G>A
ENST00000582137.6:c.*31G>A	ENSP00000462922.1:n.*31G>A
ENST00000638193.1:c.1111G>A	ENSP00000491928.1:p.Val371Met
ENST00000638276.1:c.*31G>A	ENSP00000491922.1:n.*31G>A
ENST00000638698.1:c.869G>A	ENSP00000491082.1:p.Arg290His
ENST00000638702.1:c.980G>A	ENSP00000491017.1:p.Arg327His
ENST00000638708.1:c.1067G>A	ENSP00000491580.1:p.Arg356His
ENST00000638888.1:c.*31G>A	ENSP00000491528.1:n.*31G>A
ENST00000639521.1:c.*243G>A	ENSP00000492087.1:n.*243G>A
ENST00000639835.1:c.1043G>A	ENSP00000492578.1:p.Arg348His
ENST00000640086.1:c.*31G>A	ENSP00000492238.1:n.*31G>A
ENST00000640397.1:c.697G>A	ENSP00000492379.1:p.Val233Met
ENST00000640679.1:c.869G>A	ENSP00000491092.1:p.Arg290His
ENST00000640827.1:c.*448G>A	ENSP00000492499.1:n.*448G>A
ENST00000640870.1:c.*184+264G>A	ENSP00000492479.1:n.*184+264G>A
ENST00000640979.1:c.937G>A	ENSP00000491485.1:p.Val313Met
ENST00000640999.1:c.1043G>A	ENSP00000491643.1:p.Arg348His
ENST00000245865.9:c.*1138G>A	ENSP00000245865.5:n.*1138G>A
ENST00000336174.10:c.1154G>A	ENSP00000336655.6:p.Arg385His
ENST00000375840.8:c.980G>A	ENSP00000365000.4:p.Arg327His
ENST00000392950.8:c.*542G>A	ENSP00000376677.4:n.*542G>A
ENST00000447001.7:c.*31G>A	ENSP00000398841.3:n.*31G>A
ENST00000580039.5:n.1005G>A
ENST00000580553.1:c.1232G>A
ENST00000582026.1:c.422G>A
ENST00000582137.5:c.*31G>A	ENSP00000462922.1:n.*31G>A
ENST00000583085.1:n.2784G>A
NM_001003786.2:c.1043G>A	NP_001003786.1:p.Arg348His
NM_001003787.2:c.1154G>A	NP_001003787.1:p.Arg385His
NM_001003788.2:c.980G>A	NP_001003788.1:p.Arg327His
NM_001165969.1:c.*31G>A	NP_001159441.1:n.*31G>A
NM_001165970.1:c.*31G>A	NP_001159442.1:n.*31G>A
NM_153335.5:c.*542G>A	NP_699166.2:n.*542G>A
XM_005257797.1:c.1130G>A	XP_005257854.1:p.Arg377His
XM_005257798.1:c.1067G>A	XP_005257855.1:p.Arg356His
XM_005257799.1:c.980G>A	XP_005257856.1:p.Arg327His
XM_005257800.1:c.*31G>A	XP_005257857.1:n.*31G>A
XM_011525466.1:c.1111G>A	XP_011523768.1:p.Val371Met
XM_011525467.1:c.1049G>A	XP_011523769.1:p.Arg350His
XR_243687.1:n.1131G>A
XR_243688.1:n.1040G>A
NM_001003786.3:c.1043G>A	NP_001003786.1:p.Arg348His
NM_001003787.3:c.1154G>A	NP_001003787.1:p.Arg385His
NM_001003788.3:c.980G>A	NP_001003788.1:p.Arg327His
NM_001165969.2:c.*31G>A	NP_001159441.1:n.*31G>A
NM_001165970.2:c.*31G>A	NP_001159442.1:n.*31G>A
NM_001363786.1:c.1130G>A	NP_001350715.1:p.Arg377His
NM_001363787.1:c.1067G>A	NP_001350716.1:p.Arg356His
NM_001363788.1:c.*31G>A	NP_001350717.1:n.*31G>A
NM_001363789.1:c.*31G>A	NP_001350718.1:n.*31G>A
NM_001363790.1:c.846G>A	NP_001350719.1:p.Thr282=
NM_001363791.1:c.*31G>A	NP_001350720.1:n.*31G>A
NM_153335.6:c.*542G>A	NP_699166.2:n.*542G>A
NR_156741.1:n.1272G>A
XM_005257799.3:c.980G>A	XP_005257856.1:p.Arg327His
XM_011525466.3:c.1111G>A	XP_011523768.1:p.Val371Met
XM_011525467.3:c.1049G>A	XP_011523769.1:p.Arg350His
XR_243688.3:n.1038G>A
NM_001003787.4:c.1154G>A MANE Select	NP_001003787.1:p.Arg385His
NR_156741.2:n.1085G>A