Canonical Allele Identifier: CA1381566492

Gene: POU1F1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87262061_87262063delinsAAT , CM000665.2:g.87262061_87262063delinsAAT	GRCh38
NC_000003.11:g.87311211_87311213delinsAAT , CM000665.1:g.87311211_87311213delinsAAT	GRCh37
NC_000003.10:g.87393901_87393903delinsAAT	NCBI36
NG_008225.2:g.19525_19527delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.682+8_682+10delinsATT	ENSP00000342931.3:n.682+8_682+10delinsATT
ENST00000350375.7:c.604+8_604+10delinsATT MANE Select	ENSP00000263781.2:n.604+8_604+10delinsATT
ENST00000344265.7:c.682+8_682+10delinsATT	ENSP00000342931.3:n.682+8_682+10delinsATT
ENST00000350375.6:c.604+8_604+10delinsATT	ENSP00000263781.2:n.604+8_604+10delinsATT
ENST00000560656.1:c.440-1959_440-1957delinsATT	ENSP00000452610.1:n.440-1959_440-1957delinsATT
ENST00000561167.5:c.379+8_379+10delinsATT	ENSP00000454072.1:n.379+8_379+10delinsATT
NM_000306.3:c.604+8_604+10delinsATT	NP_000297.1:n.604+8_604+10delinsATT
NM_001122757.2:c.682+8_682+10delinsATT	NP_001116229.1:n.682+8_682+10delinsATT
NM_000306.4:c.604+8_604+10delinsATT MANE Select	NP_000297.1:n.604+8_604+10delinsATT
NM_001122757.3:c.682+8_682+10delinsATT	NP_001116229.1:n.682+8_682+10delinsATT