Canonical Allele Identifier: CA136804079

Gene: PSORS1C1 CDSN

Linked Data

• dbSNP Id: rs121917819
• MyVariant Identifiers: chr6:g.31084749G>C (hg19) ; chr6:g.31116972G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31116972G>C , CM000668.2:g.31116972G>C	GRCh38
NC_000006.11:g.31084749G>C , CM000668.1:g.31084749G>C	GRCh37
NC_000006.10:g.31192728G>C	NCBI36
NG_012192.1:g.8475C>G
NG_021348.1:g.7142G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000259881.10:c.-229+2081G>C (PSORS1C1) MANE Select	ENSP00000259881.9:n.-229+2081G>C
ENST00000376288.3:c.643C>G (CDSN) MANE Select	ENSP00000365465.2:p.Gln215Glu
ENST00000259881.9:c.-229+2081G>C (PSORS1C1)	ENSP00000259881.9:n.-229+2081G>C
ENST00000376288.2:c.643C>G (CDSN)	ENSP00000365465.2:p.Gln215Glu
ENST00000467107.1:n.1979G>C (PSORS1C1)
ENST00000479581.5:n.61+2081G>C (PSORS1C1)
ENST00000493289.1:n.68-118G>C (PSORS1C1)
ENST00000548049.1:n.119+2081G>C (PSORS1C1)
ENST00000550838.1:n.58+2081G>C (PSORS1C1)
ENST00000552747.1:n.53+2081G>C (PSORS1C1)
NM_001264.4:c.643C>G (CDSN)	NP_001255.3:p.Gln215Glu
NM_014068.2:c.-229+2081G>C (PSORS1C1)	NP_054787.2:n.-229+2081G>C
NM_001264.5:c.643C>G (CDSN) MANE Select	NP_001255.4:p.Gln215Glu
NM_014068.3:c.-229+2081G>C (PSORS1C1) MANE Select	NP_054787.2:n.-229+2081G>C