Canonical Allele Identifier: CA372064305

Gene: TRPS1

Linked Data

• ClinVar Variation Id: 438463
• ClinVar RCV Id: RCV000505344 ; RCV000805667 ; RCV001268213
• dbSNP Id: rs751565386
• gnomAD v4: 8-115418392-G-A
• COSMIC: COSM4736678 ; COSM4736679
• MyVariant Identifiers: chr8:g.116430620G>A (hg19) ; chr8:g.115418392G>A (hg38)
• PubMed: PMID:25792522 ; PMID:28426188

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.115418392G>A , CM000670.2:g.115418392G>A	GRCh38
NC_000008.10:g.116430620G>A , CM000670.1:g.116430620G>A	GRCh37
NC_000008.9:g.116499796G>A	NCBI36
NG_012383.3:g.255610C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395715.8:c.2761C>T MANE Select	ENSP00000379065.3:p.Arg921Ter
ENST00000640765.1:c.2722C>T	ENSP00000492037.1:p.Arg908Ter
ENST00000220888.9:c.2722C>T	ENSP00000220888.5:p.Arg908Ter
ENST00000395715.7:c.2761C>T	ENSP00000379065.3:p.Arg921Ter
ENST00000518018.1:c.95C>T
ENST00000519076.5:c.1984C>T	ENSP00000428910.1:p.Arg662Ter
ENST00000520276.5:c.2734C>T	ENSP00000428680.1:p.Arg912Ter
NM_001282902.2:c.2734C>T	NP_001269831.1:p.Arg912Ter
NM_001282903.2:c.2740C>T	NP_001269832.1:p.Arg914Ter
NM_014112.4:c.2761C>T	NP_054831.2:p.Arg921Ter
XM_005251049.2:c.2722C>T	XP_005251106.1:p.Arg908Ter
XM_006716625.1:c.2761C>T	XP_006716688.1:p.Arg921Ter
XM_011517264.1:c.2761C>T	XP_011515566.1:p.Arg921Ter
XM_011517265.1:c.2761C>T	XP_011515567.1:p.Arg921Ter
XM_011517266.1:c.2761C>T	XP_011515568.1:p.Arg921Ter
XM_011517267.1:c.2740C>T	XP_011515569.1:p.Arg914Ter
XM_011517268.1:c.2722C>T	XP_011515570.1:p.Arg908Ter
NM_001330599.1:c.2722C>T	NP_001317528.1:p.Arg908Ter
XM_011517264.2:c.2761C>T	XP_011515566.1:p.Arg921Ter
XM_011517266.3:c.2761C>T	XP_011515568.1:p.Arg921Ter
XM_011517268.2:c.2722C>T	XP_011515570.1:p.Arg908Ter
NM_001282902.3:c.2734C>T	NP_001269831.1:p.Arg912Ter
NM_001282903.3:c.2740C>T	NP_001269832.1:p.Arg914Ter
NM_001330599.2:c.2722C>T	NP_001317528.1:p.Arg908Ter
NM_014112.5:c.2761C>T MANE Select	NP_054831.2:p.Arg921Ter