Canonical Allele Identifier: CA1619021449

Gene: PSORS1C1 PSORS1C2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31139068G= , CM000668.2:g.31139068G=	GRCh38
NC_000006.11:g.31106845G= , CM000668.1:g.31106845G=	GRCh37
NC_000006.10:g.31214824G=	NCBI36
NG_021348.1:g.29238G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259881.10:c.167+289G= (PSORS1C1) MANE Select	ENSP00000259881.9:n.167+289G=
ENST00000259845.4:c.-42C= (PSORS1C2)	ENSP00000259845.4:n.-42C=
ENST00000259881.9:c.167+289G= (PSORS1C1)	ENSP00000259881.9:n.167+289G=
ENST00000479581.5:n.62-573G= (PSORS1C1)
ENST00000481450.2:c.-22-573G= (PSORS1C1)	ENSP00000447158.1:n.-22-573G=
ENST00000547221.1:c.23+289G= (PSORS1C1)	ENSP00000449471.1:n.23+289G=
ENST00000552747.1:n.763G= (PSORS1C1)
NM_014068.2:c.167+289G= (PSORS1C1)	NP_054787.2:n.167+289G=
NM_014069.2:c.-42C= (PSORS1C2)	NP_054788.2:n.-42C=
NM_014068.3:c.167+289G= (PSORS1C1) MANE Select	NP_054787.2:n.167+289G=