Canonical Allele Identifier: CA2677932497
Gene: PSORS1C1 HGNC NCBI
PSORS1C2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31139292_31139293insTTAATGA , CM000668.2:g.31139292_31139293insTTAATGA GRCh38
NC_000006.11:g.31107069_31107070insTTAATGA , CM000668.1:g.31107069_31107070insTTAATGA GRCh37
NC_000006.10:g.31215048_31215049insTTAATGA NCBI36
NG_021348.1:g.29462_29463insTTAATGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000259881.10:c.168-349_168-348insTTAATGA (PSORS1C1) MANE Select ENSP00000259881.9:n.168-349_168-348insTTAATGA
ENST00000259845.4:c.-267_-266insTCATTAA (PSORS1C2) ENSP00000259845.4:n.-267_-266insTCATTAA
ENST00000259881.9:c.168-349_168-348insTTAATGA (PSORS1C1) ENSP00000259881.9:n.168-349_168-348insTTAATGA
ENST00000479581.5:n.62-349_62-348insTTAATGA (PSORS1C1)
ENST00000481450.2:c.-22-349_-22-348insTTAATGA (PSORS1C1) ENSP00000447158.1:n.-22-349_-22-348insTTAATGA
ENST00000547221.1:c.24-349_24-348insTTAATGA (PSORS1C1) ENSP00000449471.1:n.24-349_24-348insTTAATGA
ENST00000552747.1:n.987_988insTTAATGA (PSORS1C1)
NM_014068.2:c.168-349_168-348insTTAATGA (PSORS1C1) NP_054787.2:n.168-349_168-348insTTAATGA
NM_014069.2:c.-267_-266insTCATTAA (PSORS1C2) NP_054788.2:n.-267_-266insTCATTAA
NM_014068.3:c.168-349_168-348insTTAATGA (PSORS1C1) MANE Select NP_054787.2:n.168-349_168-348insTTAATGA