Canonical Allele Identifier: CA2677931967

Gene: PSORS1C2 PSORS1C1

Linked Data

• gnomAD v4: 6-31139058-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31139058G>T , CM000668.2:g.31139058G>T	GRCh38
NC_000006.11:g.31106835G>T , CM000668.1:g.31106835G>T	GRCh37
NC_000006.10:g.31214814G>T	NCBI36
NG_021348.1:g.29228G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000259845.5:c.-32C>A (PSORS1C2) MANE Select	ENSP00000259845.4:n.-32C>A
ENST00000259881.10:c.167+279G>T (PSORS1C1) MANE Select	ENSP00000259881.9:n.167+279G>T
ENST00000259845.4:c.-32C>A (PSORS1C2)	ENSP00000259845.4:n.-32C>A
ENST00000259881.9:c.167+279G>T (PSORS1C1)	ENSP00000259881.9:n.167+279G>T
ENST00000479581.5:n.62-583G>T (PSORS1C1)
ENST00000481450.2:c.-22-583G>T (PSORS1C1)	ENSP00000447158.1:n.-22-583G>T
ENST00000547221.1:c.23+279G>T (PSORS1C1)	ENSP00000449471.1:n.23+279G>T
ENST00000552747.1:n.753G>T (PSORS1C1)
NM_014068.2:c.167+279G>T (PSORS1C1)	NP_054787.2:n.167+279G>T
NM_014069.2:c.-32C>A (PSORS1C2)	NP_054788.2:n.-32C>A
NM_014069.3:c.-32C>A (PSORS1C2) MANE Select	NP_054788.2:n.-32C>A
NM_014068.3:c.167+279G>T (PSORS1C1) MANE Select	NP_054787.2:n.167+279G>T