Canonical Allele Identifier: CA2677932578
Gene: PSORS1C1 HGNC NCBI
PSORS1C2 HGNC NCBI

Linked Data

gnomAD v4: 6-31139306-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31139306C>G , CM000668.2:g.31139306C>G GRCh38
NC_000006.11:g.31107083C>G , CM000668.1:g.31107083C>G GRCh37
NC_000006.10:g.31215062C>G NCBI36
NG_021348.1:g.29476C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000259881.10:c.168-335C>G (PSORS1C1) MANE Select ENSP00000259881.9:n.168-335C>G
ENST00000259845.4:c.-280G>C (PSORS1C2) ENSP00000259845.4:n.-280G>C
ENST00000259881.9:c.168-335C>G (PSORS1C1) ENSP00000259881.9:n.168-335C>G
ENST00000479581.5:n.62-335C>G (PSORS1C1)
ENST00000481450.2:c.-22-335C>G (PSORS1C1) ENSP00000447158.1:n.-22-335C>G
ENST00000547221.1:c.24-335C>G (PSORS1C1) ENSP00000449471.1:n.24-335C>G
ENST00000552747.1:n.1001C>G (PSORS1C1)
NM_014068.2:c.168-335C>G (PSORS1C1) NP_054787.2:n.168-335C>G
NM_014069.2:c.-280G>C (PSORS1C2) NP_054788.2:n.-280G>C
NM_014068.3:c.168-335C>G (PSORS1C1) MANE Select NP_054787.2:n.168-335C>G