Canonical Allele Identifier: CA1812853700
Gene: TRPS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.115414180T= , CM000670.2:g.115414180T= GRCh38
NC_000008.10:g.116426408T= , CM000670.1:g.116426408T= GRCh37
NC_000008.9:g.116495584T= NCBI36
NG_012383.3:g.259822A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395715.8:c.3728A= MANE Select ENSP00000379065.3:p.Tyr1243=
ENST00000640765.1:c.3689A= ENSP00000492037.1:p.Tyr1230=
ENST00000220888.9:c.3689A= ENSP00000220888.5:p.Tyr1230=
ENST00000395715.7:c.3728A= ENSP00000379065.3:p.Tyr1243=
ENST00000519076.5:c.2951A= ENSP00000428910.1:p.Tyr984=
ENST00000520276.5:c.3701A= ENSP00000428680.1:p.Tyr1234=
NM_001282902.2:c.3701A= NP_001269831.1:p.Tyr1234=
NM_001282903.2:c.3707A= NP_001269832.1:p.Tyr1236=
NM_014112.4:c.3728A= NP_054831.2:p.Tyr1243=
XM_005251049.2:c.3689A= XP_005251106.1:p.Tyr1230=
XM_006716625.1:c.3728A= XP_006716688.1:p.Tyr1243=
XM_011517264.1:c.3728A= XP_011515566.1:p.Tyr1243=
XM_011517265.1:c.3728A= XP_011515567.1:p.Tyr1243=
XM_011517266.1:c.3728A= XP_011515568.1:p.Tyr1243=
XM_011517267.1:c.3707A= XP_011515569.1:p.Tyr1236=
XM_011517268.1:c.3689A= XP_011515570.1:p.Tyr1230=
NM_001330599.1:c.3689A= NP_001317528.1:p.Tyr1230=
XM_011517264.2:c.3728A= XP_011515566.1:p.Tyr1243=
XM_011517266.3:c.3728A= XP_011515568.1:p.Tyr1243=
XM_011517268.2:c.3689A= XP_011515570.1:p.Tyr1230=
NM_001282902.3:c.3701A= NP_001269831.1:p.Tyr1234=
NM_001282903.3:c.3707A= NP_001269832.1:p.Tyr1236=
NM_001330599.2:c.3689A= NP_001317528.1:p.Tyr1230=
NM_014112.5:c.3728A= MANE Select NP_054831.2:p.Tyr1243=