Canonical Allele Identifier: CA1381566402

Gene: POU1F1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87261958_87261968delinsGAAAAGGCGGA , CM000665.2:g.87261958_87261968delinsGAAAAGGCGGA	GRCh38
NC_000003.11:g.87311108_87311118delinsGAAAAGGCGGA , CM000665.1:g.87311108_87311118delinsGAAAAGGCGGA	GRCh37
NC_000003.10:g.87393798_87393808delinsGAAAAGGCGGA	NCBI36
NG_008225.2:g.19620_19630delinsTCCGCCTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.682+103_682+113delinsTCCGCCTTTTC	ENSP00000342931.3:n.682+103_682+113delinsTCCGCCTTTTC
ENST00000350375.7:c.604+103_604+113delinsTCCGCCTTTTC MANE Select	ENSP00000263781.2:n.604+103_604+113delinsTCCGCCTTTTC
ENST00000344265.7:c.682+103_682+113delinsTCCGCCTTTTC	ENSP00000342931.3:n.682+103_682+113delinsTCCGCCTTTTC
ENST00000350375.6:c.604+103_604+113delinsTCCGCCTTTTC	ENSP00000263781.2:n.604+103_604+113delinsTCCGCCTTTTC
ENST00000560656.1:c.440-1864_440-1854delinsTCCGCCTTTTC	ENSP00000452610.1:n.440-1864_440-1854delinsTCCGCCTTTTC
ENST00000561167.5:c.379+103_379+113delinsTCCGCCTTTTC	ENSP00000454072.1:n.379+103_379+113delinsTCCGCCTTTTC
NM_000306.3:c.604+103_604+113delinsTCCGCCTTTTC	NP_000297.1:n.604+103_604+113delinsTCCGCCTTTTC
NM_001122757.2:c.682+103_682+113delinsTCCGCCTTTTC	NP_001116229.1:n.682+103_682+113delinsTCCGCCTTTTC
NM_000306.4:c.604+103_604+113delinsTCCGCCTTTTC MANE Select	NP_000297.1:n.604+103_604+113delinsTCCGCCTTTTC
NM_001122757.3:c.682+103_682+113delinsTCCGCCTTTTC	NP_001116229.1:n.682+103_682+113delinsTCCGCCTTTTC