Canonical Allele Identifier: CA16043431
Gene: TRPS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 374202
ClinVar RCV Id: RCV000415011 RCV000505377 RCV000695017
dbSNP Id: rs1057518972
MyVariant Identifiers: chr8:g.116430587C>T (hg19) chr8:g.115418359C>T (hg38)
PubMed: PMID:25792522 PMID:28426188
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.115418359C>T , CM000670.2:g.115418359C>T GRCh38
NC_000008.10:g.116430587C>T , CM000670.1:g.116430587C>T GRCh37
NC_000008.9:g.116499763C>T NCBI36
NG_012383.3:g.255643G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000395715.8:c.2794G>A MANE Select ENSP00000379065.3:p.Ala932Thr
ENST00000640765.1:c.2755G>A ENSP00000492037.1:p.Ala919Thr
ENST00000220888.9:c.2755G>A ENSP00000220888.5:p.Ala919Thr
ENST00000395715.7:c.2794G>A ENSP00000379065.3:p.Ala932Thr
ENST00000518018.1:c.128G>A
ENST00000519076.5:c.2017G>A ENSP00000428910.1:p.Ala673Thr
ENST00000520276.5:c.2767G>A ENSP00000428680.1:p.Ala923Thr
NM_001282902.2:c.2767G>A NP_001269831.1:p.Ala923Thr
NM_001282903.2:c.2773G>A NP_001269832.1:p.Ala925Thr
NM_014112.4:c.2794G>A NP_054831.2:p.Ala932Thr
XM_005251049.2:c.2755G>A XP_005251106.1:p.Ala919Thr
XM_006716625.1:c.2794G>A XP_006716688.1:p.Ala932Thr
XM_011517264.1:c.2794G>A XP_011515566.1:p.Ala932Thr
XM_011517265.1:c.2794G>A XP_011515567.1:p.Ala932Thr
XM_011517266.1:c.2794G>A XP_011515568.1:p.Ala932Thr
XM_011517267.1:c.2773G>A XP_011515569.1:p.Ala925Thr
XM_011517268.1:c.2755G>A XP_011515570.1:p.Ala919Thr
NM_001330599.1:c.2755G>A NP_001317528.1:p.Ala919Thr
XM_011517264.2:c.2794G>A XP_011515566.1:p.Ala932Thr
XM_011517266.3:c.2794G>A XP_011515568.1:p.Ala932Thr
XM_011517268.2:c.2755G>A XP_011515570.1:p.Ala919Thr
NM_001282902.3:c.2767G>A NP_001269831.1:p.Ala923Thr
NM_001282903.3:c.2773G>A NP_001269832.1:p.Ala925Thr
NM_001330599.2:c.2755G>A NP_001317528.1:p.Ala919Thr
NM_014112.5:c.2794G>A MANE Select NP_054831.2:p.Ala932Thr
Search 100 bp 5'
Search 100 bp 3'