Canonical Allele Identifier: CA2578563747
Gene: PSORS1C2 HGNC NCBI
PSORS1C1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31139034dup , CM000668.2:g.31139034dup GRCh38
NC_000006.11:g.31106811dup , CM000668.1:g.31106811dup GRCh37
NC_000006.10:g.31214790dup NCBI36
NG_021348.1:g.29204dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000259845.5:c.-8dup (PSORS1C2) MANE Select ENSP00000259845.4:n.-8dup
ENST00000259881.10:c.167+255dup (PSORS1C1) MANE Select ENSP00000259881.9:n.167+255dup
ENST00000259845.4:c.-8dup (PSORS1C2) ENSP00000259845.4:n.-8dup
ENST00000259881.9:c.167+255dup (PSORS1C1) ENSP00000259881.9:n.167+255dup
ENST00000479581.5:n.62-607dup (PSORS1C1)
ENST00000481450.2:c.-23+575dup (PSORS1C1) ENSP00000447158.1:n.-23+575dup
ENST00000547221.1:c.23+255dup (PSORS1C1) ENSP00000449471.1:n.23+255dup
ENST00000552747.1:n.729dup (PSORS1C1)
NM_014068.2:c.167+255dup (PSORS1C1) NP_054787.2:n.167+255dup
NM_014069.2:c.-8dup (PSORS1C2) NP_054788.2:n.-8dup
NM_014069.3:c.-8dup (PSORS1C2) MANE Select NP_054788.2:n.-8dup
NM_014068.3:c.167+255dup (PSORS1C1) MANE Select NP_054787.2:n.167+255dup