Canonical Allele Identifier: CA1381566485

Gene: POU1F1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87262042_87262057delinsGCACAGCCTTCAGAGA , CM000665.2:g.87262042_87262057delinsGCACAGCCTTCAGAGA	GRCh38
NC_000003.11:g.87311192_87311207delinsGCACAGCCTTCAGAGA , CM000665.1:g.87311192_87311207delinsGCACAGCCTTCAGAGA	GRCh37
NC_000003.10:g.87393882_87393897delinsGCACAGCCTTCAGAGA	NCBI36
NG_008225.2:g.19531_19546delinsTCTCTGAAGGCTGTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.682+14_682+29delinsTCTCTGAAGGCTGTGC	ENSP00000342931.3:n.682+14_682+29delinsTCTCTGAAGGCTGTGC
ENST00000350375.7:c.604+14_604+29delinsTCTCTGAAGGCTGTGC MANE Select	ENSP00000263781.2:n.604+14_604+29delinsTCTCTGAAGGCTGTGC
ENST00000344265.7:c.682+14_682+29delinsTCTCTGAAGGCTGTGC	ENSP00000342931.3:n.682+14_682+29delinsTCTCTGAAGGCTGTGC
ENST00000350375.6:c.604+14_604+29delinsTCTCTGAAGGCTGTGC	ENSP00000263781.2:n.604+14_604+29delinsTCTCTGAAGGCTGTGC
ENST00000560656.1:c.440-1953_440-1938delinsTCTCTGAAGGCTGTGC	ENSP00000452610.1:n.440-1953_440-1938delinsTCTCTGAAGGCTGTGC
ENST00000561167.5:c.379+14_379+29delinsTCTCTGAAGGCTGTGC	ENSP00000454072.1:n.379+14_379+29delinsTCTCTGAAGGCTGTGC
NM_000306.3:c.604+14_604+29delinsTCTCTGAAGGCTGTGC	NP_000297.1:n.604+14_604+29delinsTCTCTGAAGGCTGTGC
NM_001122757.2:c.682+14_682+29delinsTCTCTGAAGGCTGTGC	NP_001116229.1:n.682+14_682+29delinsTCTCTGAAGGCTGTGC
NM_000306.4:c.604+14_604+29delinsTCTCTGAAGGCTGTGC MANE Select	NP_000297.1:n.604+14_604+29delinsTCTCTGAAGGCTGTGC
NM_001122757.3:c.682+14_682+29delinsTCTCTGAAGGCTGTGC	NP_001116229.1:n.682+14_682+29delinsTCTCTGAAGGCTGTGC