Canonical Allele Identifier: CA1087441833

Gene: PSORS1C1 PSORS1C2

Linked Data

• dbSNP Id: rs1773329534
• gnomAD v3: 6-31139322-C-T
• gnomAD v4: 6-31139322-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31139322C>T , CM000668.2:g.31139322C>T	GRCh38
NC_000006.11:g.31107099C>T , CM000668.1:g.31107099C>T	GRCh37
NC_000006.10:g.31215078C>T	NCBI36
NG_021348.1:g.29492C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259881.10:c.168-319C>T (PSORS1C1) MANE Select	ENSP00000259881.9:n.168-319C>T
ENST00000259845.4:c.-296G>A (PSORS1C2)	ENSP00000259845.4:n.-296G>A
ENST00000259881.9:c.168-319C>T (PSORS1C1)	ENSP00000259881.9:n.168-319C>T
ENST00000479581.5:n.62-319C>T (PSORS1C1)
ENST00000481450.2:c.-22-319C>T (PSORS1C1)	ENSP00000447158.1:n.-22-319C>T
ENST00000547221.1:c.24-319C>T (PSORS1C1)	ENSP00000449471.1:n.24-319C>T
ENST00000552747.1:n.1017C>T (PSORS1C1)
NM_014068.2:c.168-319C>T (PSORS1C1)	NP_054787.2:n.168-319C>T
NM_014069.2:c.-296G>A (PSORS1C2)	NP_054788.2:n.-296G>A
NM_014068.3:c.168-319C>T (PSORS1C1) MANE Select	NP_054787.2:n.168-319C>T