Canonical Allele Identifier: CA449788016

Gene: PSORS1C1 CDSN

Linked Data

• dbSNP Id: rs1398040698
• gnomAD v2: 6-31085284-G-A
• gnomAD v4: 6-31117507-G-A
• MyVariant Identifiers: chr6:g.31085284G>A (hg19) ; chr6:g.31117507G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31117507G>A , CM000668.2:g.31117507G>A	GRCh38
NC_000006.11:g.31085284G>A , CM000668.1:g.31085284G>A	GRCh37
NC_000006.10:g.31193263G>A	NCBI36
NG_012192.1:g.7940C>T
NG_021348.1:g.7677G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259881.10:c.-229+2616G>A (PSORS1C1) MANE Select	ENSP00000259881.9:n.-229+2616G>A
ENST00000376288.3:c.108C>T (CDSN) MANE Select	ENSP00000365465.2:p.Gly36=
ENST00000259881.9:c.-229+2616G>A (PSORS1C1)	ENSP00000259881.9:n.-229+2616G>A
ENST00000376288.2:c.108C>T (CDSN)	ENSP00000365465.2:p.Gly36=
ENST00000467107.1:n.2514G>A (PSORS1C1)
ENST00000479581.5:n.61+2616G>A (PSORS1C1)
ENST00000548049.1:n.119+2616G>A (PSORS1C1)
ENST00000550838.1:n.58+2616G>A (PSORS1C1)
ENST00000552747.1:n.53+2616G>A (PSORS1C1)
NM_001264.4:c.108C>T (CDSN)	NP_001255.3:p.Gly36=
NM_014068.2:c.-229+2616G>A (PSORS1C1)	NP_054787.2:n.-229+2616G>A
NM_001264.5:c.108C>T (CDSN) MANE Select	NP_001255.4:p.Gly36=
NM_014068.3:c.-229+2616G>A (PSORS1C1) MANE Select	NP_054787.2:n.-229+2616G>A