Canonical Allele Identifier: CA1812857618
Gene: TRPS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.115418470A= , CM000670.2:g.115418470A= GRCh38
NC_000008.10:g.116430698A= , CM000670.1:g.116430698A= GRCh37
NC_000008.9:g.116499874A= NCBI36
NG_012383.3:g.255532T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395715.8:c.2701-18T= MANE Select ENSP00000379065.3:n.2701-18T=
ENST00000640765.1:c.2662-18T= ENSP00000492037.1:n.2662-18T=
ENST00000220888.9:c.2662-18T= ENSP00000220888.5:n.2662-18T=
ENST00000395715.7:c.2701-18T= ENSP00000379065.3:n.2701-18T=
ENST00000518018.1:c.35-18T=
ENST00000519076.5:c.1924-18T= ENSP00000428910.1:n.1924-18T=
ENST00000520276.5:c.2674-18T= ENSP00000428680.1:n.2674-18T=
NM_001282902.2:c.2674-18T= NP_001269831.1:n.2674-18T=
NM_001282903.2:c.2680-18T= NP_001269832.1:n.2680-18T=
NM_014112.4:c.2701-18T= NP_054831.2:n.2701-18T=
XM_005251049.2:c.2662-18T= XP_005251106.1:n.2662-18T=
XM_006716625.1:c.2701-18T= XP_006716688.1:n.2701-18T=
XM_011517264.1:c.2701-18T= XP_011515566.1:n.2701-18T=
XM_011517265.1:c.2701-18T= XP_011515567.1:n.2701-18T=
XM_011517266.1:c.2701-18T= XP_011515568.1:n.2701-18T=
XM_011517267.1:c.2680-18T= XP_011515569.1:n.2680-18T=
XM_011517268.1:c.2662-18T= XP_011515570.1:n.2662-18T=
NM_001330599.1:c.2662-18T= NP_001317528.1:n.2662-18T=
XM_011517264.2:c.2701-18T= XP_011515566.1:n.2701-18T=
XM_011517266.3:c.2701-18T= XP_011515568.1:n.2701-18T=
XM_011517268.2:c.2662-18T= XP_011515570.1:n.2662-18T=
NM_001282902.3:c.2674-18T= NP_001269831.1:n.2674-18T=
NM_001282903.3:c.2680-18T= NP_001269832.1:n.2680-18T=
NM_001330599.2:c.2662-18T= NP_001317528.1:n.2662-18T=
NM_014112.5:c.2701-18T= MANE Select NP_054831.2:n.2701-18T=