Canonical Allele Identifier: CA2677932025
Gene: PSORS1C1 HGNC NCBI
PSORS1C2 HGNC NCBI

Linked Data

gnomAD v4: 6-31139105-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31139105G>C , CM000668.2:g.31139105G>C GRCh38
NC_000006.11:g.31106882G>C , CM000668.1:g.31106882G>C GRCh37
NC_000006.10:g.31214861G>C NCBI36
NG_021348.1:g.29275G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000259881.10:c.167+326G>C (PSORS1C1) MANE Select ENSP00000259881.9:n.167+326G>C
ENST00000259845.4:c.-79C>G (PSORS1C2) ENSP00000259845.4:n.-79C>G
ENST00000259881.9:c.167+326G>C (PSORS1C1) ENSP00000259881.9:n.167+326G>C
ENST00000479581.5:n.62-536G>C (PSORS1C1)
ENST00000481450.2:c.-22-536G>C (PSORS1C1) ENSP00000447158.1:n.-22-536G>C
ENST00000547221.1:c.23+326G>C (PSORS1C1) ENSP00000449471.1:n.23+326G>C
ENST00000552747.1:n.800G>C (PSORS1C1)
NM_014068.2:c.167+326G>C (PSORS1C1) NP_054787.2:n.167+326G>C
NM_014069.2:c.-79C>G (PSORS1C2) NP_054788.2:n.-79C>G
NM_014068.3:c.167+326G>C (PSORS1C1) MANE Select NP_054787.2:n.167+326G>C