Canonical Allele Identifier: CA1619021539

Gene: PSORS1C1 PSORS1C2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31139304T= , CM000668.2:g.31139304T=	GRCh38
NC_000006.11:g.31107081T= , CM000668.1:g.31107081T=	GRCh37
NC_000006.10:g.31215060T=	NCBI36
NG_021348.1:g.29474T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259881.10:c.168-337T= (PSORS1C1) MANE Select	ENSP00000259881.9:n.168-337T=
ENST00000259845.4:c.-278A= (PSORS1C2)	ENSP00000259845.4:n.-278A=
ENST00000259881.9:c.168-337T= (PSORS1C1)	ENSP00000259881.9:n.168-337T=
ENST00000479581.5:n.62-337T= (PSORS1C1)
ENST00000481450.2:c.-22-337T= (PSORS1C1)	ENSP00000447158.1:n.-22-337T=
ENST00000547221.1:c.24-337T= (PSORS1C1)	ENSP00000449471.1:n.24-337T=
ENST00000552747.1:n.999T= (PSORS1C1)
NM_014068.2:c.168-337T= (PSORS1C1)	NP_054787.2:n.168-337T=
NM_014069.2:c.-278A= (PSORS1C2)	NP_054788.2:n.-278A=
NM_014068.3:c.168-337T= (PSORS1C1) MANE Select	NP_054787.2:n.168-337T=