Canonical Allele Identifier: CA4851447
Gene: TRPS1 HGNC NCBI

Linked Data

dbSNP Id: rs747851006

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.115414119A>T , CM000670.2:g.115414119A>T GRCh38
NC_000008.10:g.116426347A>T , CM000670.1:g.116426347A>T GRCh37
NC_000008.9:g.116495523A>T NCBI36
NG_012383.3:g.259883T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395715.8:c.3789T>A MANE Select ENSP00000379065.3:p.His1263Gln
ENST00000640765.1:c.3750T>A ENSP00000492037.1:p.His1250Gln
ENST00000220888.9:c.3750T>A ENSP00000220888.5:p.His1250Gln
ENST00000395715.7:c.3789T>A ENSP00000379065.3:p.His1263Gln
ENST00000519076.5:c.3012T>A ENSP00000428910.1:p.His1004Gln
ENST00000520276.5:c.3762T>A ENSP00000428680.1:p.His1254Gln
NM_001282902.2:c.3762T>A NP_001269831.1:p.His1254Gln
NM_001282903.2:c.3768T>A NP_001269832.1:p.His1256Gln
NM_014112.4:c.3789T>A NP_054831.2:p.His1263Gln
XM_005251049.2:c.3750T>A XP_005251106.1:p.His1250Gln
XM_006716625.1:c.3789T>A XP_006716688.1:p.His1263Gln
XM_011517264.1:c.3789T>A XP_011515566.1:p.His1263Gln
XM_011517265.1:c.3789T>A XP_011515567.1:p.His1263Gln
XM_011517266.1:c.3789T>A XP_011515568.1:p.His1263Gln
XM_011517267.1:c.3768T>A XP_011515569.1:p.His1256Gln
XM_011517268.1:c.3750T>A XP_011515570.1:p.His1250Gln
NM_001330599.1:c.3750T>A NP_001317528.1:p.His1250Gln
XM_011517264.2:c.3789T>A XP_011515566.1:p.His1263Gln
XM_011517266.3:c.3789T>A XP_011515568.1:p.His1263Gln
XM_011517268.2:c.3750T>A XP_011515570.1:p.His1250Gln
NM_001282902.3:c.3762T>A NP_001269831.1:p.His1254Gln
NM_001282903.3:c.3768T>A NP_001269832.1:p.His1256Gln
NM_001330599.2:c.3750T>A NP_001317528.1:p.His1250Gln
NM_014112.5:c.3789T>A MANE Select NP_054831.2:p.His1263Gln