Canonical Allele Identifier: CA2677932662
Gene: PSORS1C1 HGNC NCBI

Linked Data

gnomAD v4: 6-31139352-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31139352G>T , CM000668.2:g.31139352G>T GRCh38
NC_000006.11:g.31107129G>T , CM000668.1:g.31107129G>T GRCh37
NC_000006.10:g.31215108G>T NCBI36
NG_021348.1:g.29522G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259881.10:c.168-289G>T MANE Select ENSP00000259881.9:n.168-289G>T
ENST00000259881.9:c.168-289G>T ENSP00000259881.9:n.168-289G>T
ENST00000479581.5:n.62-289G>T
ENST00000481450.2:c.-22-289G>T ENSP00000447158.1:n.-22-289G>T
ENST00000547221.1:c.24-289G>T ENSP00000449471.1:n.24-289G>T
ENST00000552747.1:n.1047G>T
NM_014068.2:c.168-289G>T NP_054787.2:n.168-289G>T
NM_014068.3:c.168-289G>T MANE Select NP_054787.2:n.168-289G>T