Canonical Allele Identifier: CA1381566481

Gene: POU1F1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87262036_87262038delinsAAC , CM000665.2:g.87262036_87262038delinsAAC	GRCh38
NC_000003.11:g.87311186_87311188delinsAAC , CM000665.1:g.87311186_87311188delinsAAC	GRCh37
NC_000003.10:g.87393876_87393878delinsAAC	NCBI36
NG_008225.2:g.19550_19552delinsGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000344265.8:c.682+33_682+35delinsGTT	ENSP00000342931.3:n.682+33_682+35delinsGT...
ENST00000350375.7:c.604+33_604+35delinsGTT MANE Select	ENSP00000263781.2:n.604+33_604+35delinsGT...
ENST00000344265.7:c.682+33_682+35delinsGTT	ENSP00000342931.3:n.682+33_682+35delinsGT...
ENST00000350375.6:c.604+33_604+35delinsGTT	ENSP00000263781.2:n.604+33_604+35delinsGT...
ENST00000560656.1:c.440-1934_440-1932delinsGTT	ENSP00000452610.1:n.440-1934_440-1932deli...
ENST00000561167.5:c.379+33_379+35delinsGTT	ENSP00000454072.1:n.379+33_379+35delinsGT...
NM_000306.3:c.604+33_604+35delinsGTT	NP_000297.1:n.604+33_604+35delinsGTT
NM_001122757.2:c.682+33_682+35delinsGTT	NP_001116229.1:n.682+33_682+35delinsGTT
NM_000306.4:c.604+33_604+35delinsGTT MANE Select	NP_000297.1:n.604+33_604+35delinsGTT
NM_001122757.3:c.682+33_682+35delinsGTT	NP_001116229.1:n.682+33_682+35delinsGTT