Canonical Allele Identifier: CA1770581638
Gene: PEBP4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22786056T= , CM000670.2:g.22786056T= GRCh38
NC_000008.10:g.22643569T= , CM000670.1:g.22643569T= GRCh37
NC_000008.9:g.22699514T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256404.8:c.357+31581A= MANE Select ENSP00000256404.6:n.357+31581A=
ENST00000256404.7:c.357+31581A= ENSP00000256404.6:n.357+31581A=
NM_144962.2:c.357+31581A= NP_659399.2:n.357+31581A=
XM_011544413.1:c.357+31581A= XP_011542715.1:n.357+31581A=
XM_011544414.1:c.357+31581A= XP_011542716.1:n.357+31581A=
NM_001363233.1:c.357+31581A= NP_001350162.1:n.357+31581A=
NM_144962.3:c.357+31581A= MANE Select NP_659399.2:n.357+31581A=
NM_001363233.2:c.357+31581A= NP_001350162.1:n.357+31581A=
Search 100 bp 5'
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