Canonical Allele Identifier: CA2677928148

Gene: PSORS1C1 CDSN

Linked Data

• gnomAD v4: 6-31117555-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31117555A>T , CM000668.2:g.31117555A>T	GRCh38
NC_000006.11:g.31085332A>T , CM000668.1:g.31085332A>T	GRCh37
NC_000006.10:g.31193311A>T	NCBI36
NG_012192.1:g.7892T>A
NG_021348.1:g.7725A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259881.10:c.-229+2664A>T (PSORS1C1) MANE Select	ENSP00000259881.9:n.-229+2664A>T
ENST00000376288.3:c.86-26T>A (CDSN) MANE Select	ENSP00000365465.2:n.86-26T>A
ENST00000259881.9:c.-229+2664A>T (PSORS1C1)	ENSP00000259881.9:n.-229+2664A>T
ENST00000376288.2:c.86-26T>A (CDSN)	ENSP00000365465.2:n.86-26T>A
ENST00000467107.1:n.2562A>T (PSORS1C1)
ENST00000479581.5:n.61+2664A>T (PSORS1C1)
ENST00000548049.1:n.119+2664A>T (PSORS1C1)
ENST00000550838.1:n.58+2664A>T (PSORS1C1)
ENST00000552747.1:n.53+2664A>T (PSORS1C1)
NM_001264.4:c.86-26T>A (CDSN)	NP_001255.3:n.86-26T>A
NM_014068.2:c.-229+2664A>T (PSORS1C1)	NP_054787.2:n.-229+2664A>T
NM_001264.5:c.86-26T>A (CDSN) MANE Select	NP_001255.4:n.86-26T>A
NM_014068.3:c.-229+2664A>T (PSORS1C1) MANE Select	NP_054787.2:n.-229+2664A>T