Canonical Allele Identifier: CA1619021435

Gene: PSORS1C2 PSORS1C1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31139032T= , CM000668.2:g.31139032T=	GRCh38
NC_000006.11:g.31106809T= , CM000668.1:g.31106809T=	GRCh37
NC_000006.10:g.31214788T=	NCBI36
NG_021348.1:g.29202T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259845.5:c.-6A= (PSORS1C2) MANE Select	ENSP00000259845.4:n.-6A=
ENST00000259881.10:c.167+253T= (PSORS1C1) MANE Select	ENSP00000259881.9:n.167+253T=
ENST00000259845.4:c.-6A= (PSORS1C2)	ENSP00000259845.4:n.-6A=
ENST00000259881.9:c.167+253T= (PSORS1C1)	ENSP00000259881.9:n.167+253T=
ENST00000479581.5:n.62-609T= (PSORS1C1)
ENST00000481450.2:c.-23+573T= (PSORS1C1)	ENSP00000447158.1:n.-23+573T=
ENST00000547221.1:c.23+253T= (PSORS1C1)	ENSP00000449471.1:n.23+253T=
ENST00000552747.1:n.727T= (PSORS1C1)
NM_014068.2:c.167+253T= (PSORS1C1)	NP_054787.2:n.167+253T=
NM_014069.2:c.-6A= (PSORS1C2)	NP_054788.2:n.-6A=
NM_014069.3:c.-6A= (PSORS1C2) MANE Select	NP_054788.2:n.-6A=
NM_014068.3:c.167+253T= (PSORS1C1) MANE Select	NP_054787.2:n.167+253T=