Canonical Allele Identifier: CA353698134

Gene: POU1F1

Linked Data

• MyVariant Identifiers: chr3:g.87309131G>C (hg19) ; chr3:g.87259981G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.87259981G>C , CM000665.2:g.87259981G>C	GRCh38
NC_000003.11:g.87309131G>C , CM000665.1:g.87309131G>C	GRCh37
NC_000003.10:g.87391821G>C	NCBI36
NG_008225.2:g.21607C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344265.8:c.867C>G	ENSP00000342931.3:p.Cys289Trp
ENST00000350375.7:c.789C>G MANE Select	ENSP00000263781.2:p.Cys263Trp
ENST00000344265.7:c.867C>G	ENSP00000342931.3:p.Cys289Trp
ENST00000350375.6:c.789C>G	ENSP00000263781.2:p.Cys263Trp
ENST00000560656.1:c.563C>G	ENSP00000452610.1:n.563C>G
ENST00000561167.5:c.564C>G	ENSP00000454072.1:p.Cys188Trp
NM_000306.3:c.789C>G	NP_000297.1:p.Cys263Trp
NM_001122757.2:c.867C>G	NP_001116229.1:p.Cys289Trp
NM_000306.4:c.789C>G MANE Select	NP_000297.1:p.Cys263Trp
NM_001122757.3:c.867C>G	NP_001116229.1:p.Cys289Trp