Canonical Allele Identifier: CA4851445
Gene: TRPS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1347607
dbSNP Id: rs376875568

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.115414111G>A , CM000670.2:g.115414111G>A GRCh38
NC_000008.10:g.116426339G>A , CM000670.1:g.116426339G>A GRCh37
NC_000008.9:g.116495515G>A NCBI36
NG_012383.3:g.259891C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395715.8:c.3797C>T MANE Select ENSP00000379065.3:p.Thr1266Met
ENST00000640765.1:c.3758C>T ENSP00000492037.1:p.Thr1253Met
ENST00000220888.9:c.3758C>T ENSP00000220888.5:p.Thr1253Met
ENST00000395715.7:c.3797C>T ENSP00000379065.3:p.Thr1266Met
ENST00000519076.5:c.3020C>T ENSP00000428910.1:p.Thr1007Met
ENST00000520276.5:c.3770C>T ENSP00000428680.1:p.Thr1257Met
NM_001282902.2:c.3770C>T NP_001269831.1:p.Thr1257Met
NM_001282903.2:c.3776C>T NP_001269832.1:p.Thr1259Met
NM_014112.4:c.3797C>T NP_054831.2:p.Thr1266Met
XM_005251049.2:c.3758C>T XP_005251106.1:p.Thr1253Met
XM_006716625.1:c.3797C>T XP_006716688.1:p.Thr1266Met
XM_011517264.1:c.3797C>T XP_011515566.1:p.Thr1266Met
XM_011517265.1:c.3797C>T XP_011515567.1:p.Thr1266Met
XM_011517266.1:c.3797C>T XP_011515568.1:p.Thr1266Met
XM_011517267.1:c.3776C>T XP_011515569.1:p.Thr1259Met
XM_011517268.1:c.3758C>T XP_011515570.1:p.Thr1253Met
NM_001330599.1:c.3758C>T NP_001317528.1:p.Thr1253Met
XM_011517264.2:c.3797C>T XP_011515566.1:p.Thr1266Met
XM_011517266.3:c.3797C>T XP_011515568.1:p.Thr1266Met
XM_011517268.2:c.3758C>T XP_011515570.1:p.Thr1253Met
NM_001282902.3:c.3770C>T NP_001269831.1:p.Thr1257Met
NM_001282903.3:c.3776C>T NP_001269832.1:p.Thr1259Met
NM_001330599.2:c.3758C>T NP_001317528.1:p.Thr1253Met
NM_014112.5:c.3797C>T MANE Select NP_054831.2:p.Thr1266Met