Canonical Allele Identifier: CA449787959

Gene: PSORS1C1 CDSN

Linked Data

• gnomAD v4: 6-31117447-G-T
• MyVariant Identifiers: chr6:g.31085224G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31117447G>T , CM000668.2:g.31117447G>T	GRCh38
NC_000006.11:g.31085224G>T , CM000668.1:g.31085224G>T	GRCh37
NC_000006.10:g.31193203G>T	NCBI36
NG_012192.1:g.8000C>A
NG_021348.1:g.7617G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259881.10:c.-229+2556G>T (PSORS1C1) MANE Select	ENSP00000259881.9:n.-229+2556G>T
ENST00000376288.3:c.168C>A (CDSN) MANE Select	ENSP00000365465.2:p.Leu56=
ENST00000259881.9:c.-229+2556G>T (PSORS1C1)	ENSP00000259881.9:n.-229+2556G>T
ENST00000376288.2:c.168C>A (CDSN)	ENSP00000365465.2:p.Leu56=
ENST00000467107.1:n.2454G>T (PSORS1C1)
ENST00000479581.5:n.61+2556G>T (PSORS1C1)
ENST00000548049.1:n.119+2556G>T (PSORS1C1)
ENST00000550838.1:n.58+2556G>T (PSORS1C1)
ENST00000552747.1:n.53+2556G>T (PSORS1C1)
NM_001264.4:c.168C>A (CDSN)	NP_001255.3:p.Leu56=
NM_014068.2:c.-229+2556G>T (PSORS1C1)	NP_054787.2:n.-229+2556G>T
NM_001264.5:c.168C>A (CDSN) MANE Select	NP_001255.4:p.Leu56=
NM_014068.3:c.-229+2556G>T (PSORS1C1) MANE Select	NP_054787.2:n.-229+2556G>T