Canonical Allele Identifier: CA1619012179

Gene: PSORS1C1 CDSN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31117463G= , CM000668.2:g.31117463G=	GRCh38
NC_000006.11:g.31085240G= , CM000668.1:g.31085240G=	GRCh37
NC_000006.10:g.31193219G=	NCBI36
NG_012192.1:g.7984C=
NG_021348.1:g.7633G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000259881.10:c.-229+2572G= (PSORS1C1) MANE Select	ENSP00000259881.9:n.-229+2572G=
ENST00000376288.3:c.152C= (CDSN) MANE Select	ENSP00000365465.2:p.Pro51=
ENST00000259881.9:c.-229+2572G= (PSORS1C1)	ENSP00000259881.9:n.-229+2572G=
ENST00000376288.2:c.152C= (CDSN)	ENSP00000365465.2:p.Pro51=
ENST00000467107.1:n.2470G= (PSORS1C1)
ENST00000479581.5:n.61+2572G= (PSORS1C1)
ENST00000548049.1:n.119+2572G= (PSORS1C1)
ENST00000550838.1:n.58+2572G= (PSORS1C1)
ENST00000552747.1:n.53+2572G= (PSORS1C1)
NM_001264.4:c.152C= (CDSN)	NP_001255.3:p.Pro51=
NM_014068.2:c.-229+2572G= (PSORS1C1)	NP_054787.2:n.-229+2572G=
NM_001264.5:c.152C= (CDSN) MANE Select	NP_001255.4:p.Pro51=
NM_014068.3:c.-229+2572G= (PSORS1C1) MANE Select	NP_054787.2:n.-229+2572G=