Canonical Allele Identifier: CA136823958

Gene: POU5F1 PSORS1C3

Linked Data

• dbSNP Id: rs35819633
• MyVariant Identifiers: chr6:g.31143716_31143717insG (hg19) ; chr6:g.31175939_31175940insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31175939_31175940insG , CM000668.2:g.31175939_31175940insG	GRCh38
NC_000006.11:g.31143716_31143717insG , CM000668.1:g.31143716_31143717insG	GRCh37
NC_000006.10:g.31251695_31251696insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441888.7:c.-184+4679_-184+4680insC (POU5F1)	ENSP00000389359.2:n.-184+4679_-184+4680insC
NR_026816.1:n.262-1670_262-1669insC (PSORS1C3)
NR_026816.2:n.554-1670_554-1669insC (PSORS1C3)
NR_152828.1:n.554-1114_554-1113insC (PSORS1C3)
NR_152829.1:n.569_570insC (PSORS1C3)
NR_152830.1:n.554-1384_554-1383insC (PSORS1C3)
NR_152831.1:n.293-1670_293-1669insC (PSORS1C3)
NR_152832.1:n.414-1670_414-1669insC (PSORS1C3)
NR_152833.1:n.554-1114_554-1113insC (PSORS1C3)
NR_152834.1:n.569_570insC (PSORS1C3)
NR_152835.1:n.293-1907_293-1906insC (PSORS1C3)
NR_152836.1:n.554-1384_554-1383insC (PSORS1C3)
NR_152837.1:n.554-1261_554-1260insC (PSORS1C3)
NR_152838.1:n.569_570insC (PSORS1C3)
NR_152839.1:n.553+1699_553+1700insC (PSORS1C3)