Canonical Allele Identifier: CA363317519

Gene: PSORS1C1 CDSN

Linked Data

• MyVariant Identifiers: chr6:g.31085220C>G (hg19) ; chr6:g.31117443C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31117443C>G , CM000668.2:g.31117443C>G	GRCh38
NC_000006.11:g.31085220C>G , CM000668.1:g.31085220C>G	GRCh37
NC_000006.10:g.31193199C>G	NCBI36
NG_012192.1:g.8004G>C
NG_021348.1:g.7613C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259881.10:c.-229+2552C>G (PSORS1C1) MANE Select	ENSP00000259881.9:n.-229+2552C>G
ENST00000376288.3:c.172G>C (CDSN) MANE Select	ENSP00000365465.2:p.Gly58Arg
ENST00000259881.9:c.-229+2552C>G (PSORS1C1)	ENSP00000259881.9:n.-229+2552C>G
ENST00000376288.2:c.172G>C (CDSN)	ENSP00000365465.2:p.Gly58Arg
ENST00000467107.1:n.2450C>G (PSORS1C1)
ENST00000479581.5:n.61+2552C>G (PSORS1C1)
ENST00000548049.1:n.119+2552C>G (PSORS1C1)
ENST00000550838.1:n.58+2552C>G (PSORS1C1)
ENST00000552747.1:n.53+2552C>G (PSORS1C1)
NM_001264.4:c.172G>C (CDSN)	NP_001255.3:p.Gly58Arg
NM_014068.2:c.-229+2552C>G (PSORS1C1)	NP_054787.2:n.-229+2552C>G
NM_001264.5:c.172G>C (CDSN) MANE Select	NP_001255.4:p.Gly58Arg
NM_014068.3:c.-229+2552C>G (PSORS1C1) MANE Select	NP_054787.2:n.-229+2552C>G