Canonical Allele Identifier: CA1619012195
Gene: PSORS1C1 HGNC NCBI
CDSN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31117490C= , CM000668.2:g.31117490C= GRCh38
NC_000006.11:g.31085267C= , CM000668.1:g.31085267C= GRCh37
NC_000006.10:g.31193246C= NCBI36
NG_012192.1:g.7957G=
NG_021348.1:g.7660C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000259881.10:c.-229+2599C= (PSORS1C1) MANE Select ENSP00000259881.9:n.-229+2599C=
ENST00000376288.3:c.125G= (CDSN) MANE Select ENSP00000365465.2:p.Cys42=
ENST00000259881.9:c.-229+2599C= (PSORS1C1) ENSP00000259881.9:n.-229+2599C=
ENST00000376288.2:c.125G= (CDSN) ENSP00000365465.2:p.Cys42=
ENST00000467107.1:n.2497C= (PSORS1C1)
ENST00000479581.5:n.61+2599C= (PSORS1C1)
ENST00000548049.1:n.119+2599C= (PSORS1C1)
ENST00000550838.1:n.58+2599C= (PSORS1C1)
ENST00000552747.1:n.53+2599C= (PSORS1C1)
NM_001264.4:c.125G= (CDSN) NP_001255.3:p.Cys42=
NM_014068.2:c.-229+2599C= (PSORS1C1) NP_054787.2:n.-229+2599C=
NM_001264.5:c.125G= (CDSN) MANE Select NP_001255.4:p.Cys42=
NM_014068.3:c.-229+2599C= (PSORS1C1) MANE Select NP_054787.2:n.-229+2599C=