Canonical Allele Identifier: CA364905106

Gene: SYNCRIP

Linked Data

• ClinVar Variation Id: 2419300
• ClinVar RCV Id: RCV003112544
• gnomAD v4: 6-85624051-T-C
• MyVariant Identifiers: chr6:g.86333769T>C (hg19) ; chr6:g.85624051T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.85624051T>C , CM000668.2:g.85624051T>C	GRCh38
NC_000006.11:g.86333769T>C , CM000668.1:g.86333769T>C	GRCh37
NC_000006.10:g.86390488T>C	NCBI36
NG_031848.1:g.24275A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710383.1:c.893A>G	ENSP00000518240.1:p.Asn298Ser
ENST00000681965.1:c.267A>G	ENSP00000507317.1:n.267A>G
ENST00000682083.1:c.728A>G	ENSP00000506859.1:p.Asn243Ser
ENST00000682106.1:n.1683A>G
ENST00000682504.1:c.434A>G	ENSP00000507623.1:p.Asn145Ser
ENST00000683074.1:c.434A>G	ENSP00000507008.1:p.Asn145Ser
ENST00000683364.1:c.728A>G	ENSP00000507791.1:p.Asn243Ser
ENST00000683436.1:c.434A>G	ENSP00000506874.1:p.Asn145Ser
ENST00000683909.1:n.1199A>G
ENST00000684220.1:c.728A>G	ENSP00000507382.1:p.Asn243Ser
ENST00000684462.1:c.434A>G	ENSP00000507581.1:p.Asn145Ser
ENST00000355238.11:c.728A>G	ENSP00000347380.6:p.Asn243Ser
ENST00000369622.8:c.728A>G MANE Select	ENSP00000358635.3:p.Asn243Ser
ENST00000444272.2:c.728A>G	ENSP00000397782.2:p.Asn243Ser
ENST00000616122.5:c.434A>G	ENSP00000484577.1:p.Asn145Ser
ENST00000676542.1:c.728A>G	ENSP00000504277.1:p.Asn243Ser
ENST00000676630.1:c.614A>G	ENSP00000503268.1:p.Asn205Ser
ENST00000676637.1:c.728A>G	ENSP00000502974.1:p.Asn243Ser
ENST00000676688.1:c.728A>G	ENSP00000504706.1:p.Asn243Ser
ENST00000677059.1:c.728A>G	ENSP00000504133.1:p.Asn243Ser
ENST00000677481.1:c.*204A>G	ENSP00000503778.1:n.*204A>G
ENST00000677514.1:c.*204A>G	ENSP00000502885.1:n.*204A>G
ENST00000677646.1:n.1299A>G
ENST00000677771.1:c.728A>G	ENSP00000504816.1:p.Asn243Ser
ENST00000678355.1:c.728A>G	ENSP00000503783.1:p.Asn243Ser
ENST00000678528.1:c.728A>G	ENSP00000503246.1:p.Asn243Ser
ENST00000678589.1:c.434A>G	ENSP00000502879.1:p.Asn145Ser
ENST00000678618.1:c.437A>G	ENSP00000504657.1:p.Asn146Ser
ENST00000678816.1:c.728A>G	ENSP00000504718.1:p.Asn243Ser
ENST00000678878.1:c.728A>G	ENSP00000504086.1:p.Asn243Ser
ENST00000678899.1:c.434A>G	ENSP00000503183.1:p.Asn145Ser
ENST00000678930.1:c.728A>G	ENSP00000504120.1:p.Asn243Ser
ENST00000355238.10:c.728A>G	ENSP00000347380.6:p.Asn243Ser
ENST00000369622.7:c.728A>G	ENSP00000358635.3:p.Asn243Ser
ENST00000616122.4:c.434A>G	ENSP00000484577.1:p.Asn145Ser
NM_001159673.1:c.434A>G	NP_001153145.1:p.Asn145Ser
NM_001159674.1:c.728A>G	NP_001153146.1:p.Asn243Ser
NM_001159675.1:c.728A>G	NP_001153147.1:p.Asn243Ser
NM_001159676.1:c.728A>G	NP_001153148.1:p.Asn243Ser
NM_001159677.1:c.728A>G	NP_001153149.1:p.Asn243Ser
NM_001253771.1:c.272A>G	NP_001240700.1:p.Asn91Ser
NM_006372.4:c.728A>G	NP_006363.4:p.Asn243Ser
XM_005248635.3:c.728A>G	XP_005248692.1:p.Asn243Ser
XM_005248636.1:c.434A>G	XP_005248693.1:p.Asn145Ser
XM_005248637.1:c.728A>G	XP_005248694.1:p.Asn243Ser
XM_005248635.4:c.728A>G	XP_005248692.1:p.Asn243Ser
XM_005248636.3:c.434A>G	XP_005248693.1:p.Asn145Ser
XM_005248637.2:c.728A>G	XP_005248694.1:p.Asn243Ser
XM_017010176.1:c.728A>G	XP_016865665.1:p.Asn243Ser
XM_017010177.1:c.728A>G	XP_016865666.1:p.Asn243Ser
XM_017010178.2:c.728A>G	XP_016865667.1:p.Asn243Ser
XM_017010179.1:c.728A>G	XP_016865668.1:p.Asn243Ser
XM_017010180.2:c.434A>G	XP_016865669.1:p.Asn145Ser
NM_001159674.2:c.728A>G	NP_001153146.1:p.Asn243Ser
NM_001159677.2:c.728A>G	NP_001153149.1:p.Asn243Ser
NM_001253771.2:c.272A>G	NP_001240700.1:p.Asn91Ser
NM_006372.5:c.728A>G MANE Select	NP_006363.4:p.Asn243Ser
NM_001159673.2:c.434A>G	NP_001153145.1:p.Asn145Ser