Canonical Allele Identifier: CA371775937
Gene: POP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.98157825G>T , CM000670.2:g.98157825G>T GRCh38
NC_000008.10:g.99170053G>T , CM000670.1:g.99170053G>T GRCh37
NC_000008.9:g.99239229G>T NCBI36
NG_052869.1:g.45533G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000401707.7:c.2629G>T MANE Select ENSP00000385787.2:p.Val877Phe
ENST00000349693.3:c.2629G>T ENSP00000339529.3:p.Val877Phe
ENST00000401707.6:c.2629G>T ENSP00000385787.2:p.Val877Phe
NM_001145860.1:c.2629G>T NP_001139332.1:p.Val877Phe
NM_001145861.1:c.2629G>T NP_001139333.1:p.Val877Phe
NM_015029.2:c.2629G>T NP_055844.2:p.Val877Phe
NM_001145860.2:c.2629G>T MANE Select NP_001139332.1:p.Val877Phe
NM_001145861.2:c.2629G>T NP_001139333.1:p.Val877Phe
NM_015029.3:c.2629G>T NP_055844.2:p.Val877Phe