Canonical Allele Identifier: CA1770581601

Gene: PEBP4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22786033_22786035delinsGCA , CM000670.2:g.22786033_22786035delinsGCA	GRCh38
NC_000008.10:g.22643546_22643548delinsGCA , CM000670.1:g.22643546_22643548delinsGCA	GRCh37
NC_000008.9:g.22699491_22699493delinsGCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256404.8:c.357+31602_357+31604delinsTGC MANE Select	ENSP00000256404.6:n.357+31602_357+31604delinsTGC
ENST00000256404.7:c.357+31602_357+31604delinsTGC	ENSP00000256404.6:n.357+31602_357+31604delinsTGC
NM_144962.2:c.357+31602_357+31604delinsTGC	NP_659399.2:n.357+31602_357+31604delinsTGC
XM_011544413.1:c.357+31602_357+31604delinsTGC	XP_011542715.1:n.357+31602_357+31604delinsTGC
XM_011544414.1:c.357+31602_357+31604delinsTGC	XP_011542716.1:n.357+31602_357+31604delinsTGC
NM_001363233.1:c.357+31602_357+31604delinsTGC	NP_001350162.1:n.357+31602_357+31604delinsTGC
NM_144962.3:c.357+31602_357+31604delinsTGC MANE Select	NP_659399.2:n.357+31602_357+31604delinsTGC
NM_001363233.2:c.357+31602_357+31604delinsTGC	NP_001350162.1:n.357+31602_357+31604delinsTGC