Canonical Allele Identifier: CA823833963
Gene: PSORS1C1 HGNC NCBI

Linked Data

dbSNP Id: rs1356677299
gnomAD v3: 6-31139519-CTA-C
gnomAD v4: 6-31139519-CTA-C
MyVariant Identifiers: chr6:g.31107297_31107298del (hg19) chr6:g.31139520_31139521del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31139520_31139521del , CM000668.2:g.31139520_31139521del GRCh38
NC_000006.11:g.31107297_31107298del , CM000668.1:g.31107297_31107298del GRCh37
NC_000006.10:g.31215276_31215277del NCBI36
NG_021348.1:g.29690_29691del

Transcript Alleles

HGVS Amino-acid Change
ENST00000259881.10:c.168-121_168-120del MANE Select ENSP00000259881.9:n.168-121_168-120del
ENST00000259881.9:c.168-121_168-120del ENSP00000259881.9:n.168-121_168-120del
ENST00000479581.5:n.62-121_62-120del
ENST00000481450.2:c.-22-121_-22-120del ENSP00000447158.1:n.-22-121_-22-120del
ENST00000547221.1:c.24-121_24-120del ENSP00000449471.1:n.24-121_24-120del
NM_014068.2:c.168-121_168-120del NP_054787.2:n.168-121_168-120del
NM_014068.3:c.168-121_168-120del MANE Select NP_054787.2:n.168-121_168-120del
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