Canonical Allele Identifier: CA16618582
Gene: TRPS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 420782
ClinVar RCV Id: RCV000481714
dbSNP Id: rs1064794697

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.115414124G>A , CM000670.2:g.115414124G>A GRCh38
NC_000008.10:g.116426352G>A , CM000670.1:g.116426352G>A GRCh37
NC_000008.9:g.116495528G>A NCBI36
NG_012383.3:g.259878C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000395715.8:c.3784C>T MANE Select ENSP00000379065.3:p.Gln1262Ter
ENST00000640765.1:c.3745C>T ENSP00000492037.1:p.Gln1249Ter
ENST00000220888.9:c.3745C>T ENSP00000220888.5:p.Gln1249Ter
ENST00000395715.7:c.3784C>T ENSP00000379065.3:p.Gln1262Ter
ENST00000519076.5:c.3007C>T ENSP00000428910.1:p.Gln1003Ter
ENST00000520276.5:c.3757C>T ENSP00000428680.1:p.Gln1253Ter
NM_001282902.2:c.3757C>T NP_001269831.1:p.Gln1253Ter
NM_001282903.2:c.3763C>T NP_001269832.1:p.Gln1255Ter
NM_014112.4:c.3784C>T NP_054831.2:p.Gln1262Ter
XM_005251049.2:c.3745C>T XP_005251106.1:p.Gln1249Ter
XM_006716625.1:c.3784C>T XP_006716688.1:p.Gln1262Ter
XM_011517264.1:c.3784C>T XP_011515566.1:p.Gln1262Ter
XM_011517265.1:c.3784C>T XP_011515567.1:p.Gln1262Ter
XM_011517266.1:c.3784C>T XP_011515568.1:p.Gln1262Ter
XM_011517267.1:c.3763C>T XP_011515569.1:p.Gln1255Ter
XM_011517268.1:c.3745C>T XP_011515570.1:p.Gln1249Ter
NM_001330599.1:c.3745C>T NP_001317528.1:p.Gln1249Ter
XM_011517264.2:c.3784C>T XP_011515566.1:p.Gln1262Ter
XM_011517266.3:c.3784C>T XP_011515568.1:p.Gln1262Ter
XM_011517268.2:c.3745C>T XP_011515570.1:p.Gln1249Ter
NM_001282902.3:c.3757C>T NP_001269831.1:p.Gln1253Ter
NM_001282903.3:c.3763C>T NP_001269832.1:p.Gln1255Ter
NM_001330599.2:c.3745C>T NP_001317528.1:p.Gln1249Ter
NM_014112.5:c.3784C>T MANE Select NP_054831.2:p.Gln1262Ter