Canonical Allele Identifier: CA449788002

Gene: PSORS1C1 CDSN

Linked Data

• dbSNP Id: rs3132552
• gnomAD v4: 6-31117492-A-T
• MyVariant Identifiers: chr6:g.31085269A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31117492A>T , CM000668.2:g.31117492A>T	GRCh38
NC_000006.11:g.31085269A>T , CM000668.1:g.31085269A>T	GRCh37
NC_000006.10:g.31193248A>T	NCBI36
NG_021348.1:g.7662A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259881.10:c.-229+2601A>T (PSORS1C1) MANE Select	ENSP00000259881.9:n.-229+2601A>T
ENST00000376288.3:c.123T>A (CDSN) MANE Select	ENSP00000365465.2:p.Pro41=
ENST00000259881.9:c.-229+2601A>T (PSORS1C1)	ENSP00000259881.9:n.-229+2601A>T
ENST00000376288.2:c.123T>A (CDSN)	ENSP00000365465.2:p.Pro41=
ENST00000467107.1:n.2499A>T (PSORS1C1)
ENST00000479581.5:n.61+2601A>T (PSORS1C1)
ENST00000548049.1:n.119+2601A>T (PSORS1C1)
ENST00000550838.1:n.58+2601A>T (PSORS1C1)
ENST00000552747.1:n.53+2601A>T (PSORS1C1)
NM_014068.2:c.-229+2601A>T (PSORS1C1)	NP_054787.2:n.-229+2601A>T
NM_001264.5:c.123T>A (CDSN) MANE Select	NP_001255.4:p.Pro41=
NM_014068.3:c.-229+2601A>T (PSORS1C1) MANE Select	NP_054787.2:n.-229+2601A>T