Canonical Allele Identifier: CA849939097

Gene: PEBP4

Linked Data

• dbSNP Id: rs1227325416
• MyVariant Identifiers: chr8:g.22643719_22643720insAATACATCTAATAA (hg19) ; chr8:g.22786206_22786207insAATACATCTAATAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22786207_22786208insATACATCTAATAAA , CM000670.2:g.22786207_22786208insATACATCTAATAAA	GRCh38
NC_000008.10:g.22643720_22643721insATACATCTAATAAA , CM000670.1:g.22643720_22643721insATACATCTAATAAA	GRCh37
NC_000008.9:g.22699665_22699666insATACATCTAATAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256404.8:c.357+31430_357+31431insTTATTAGATGTATT MANE Select	ENSP00000256404.6:n.357+31430_357+31431insTTATTAGATGTATT
ENST00000256404.7:c.357+31430_357+31431insTTATTAGATGTATT	ENSP00000256404.6:n.357+31430_357+31431insTTATTAGATGTATT
NM_144962.2:c.357+31430_357+31431insTTATTAGATGTATT	NP_659399.2:n.357+31430_357+31431insTTATTAGATGTATT
XM_011544413.1:c.357+31430_357+31431insTTATTAGATGTATT	XP_011542715.1:n.357+31430_357+31431insTTATTAGATGTATT
XM_011544414.1:c.357+31430_357+31431insTTATTAGATGTATT	XP_011542716.1:n.357+31430_357+31431insTTATTAGATGTATT
NM_001363233.1:c.357+31430_357+31431insTTATTAGATGTATT	NP_001350162.1:n.357+31430_357+31431insTTATTAGATGTATT
NM_144962.3:c.357+31430_357+31431insTTATTAGATGTATT MANE Select	NP_659399.2:n.357+31430_357+31431insTTATTAGATGTATT
NM_001363233.2:c.357+31430_357+31431insTTATTAGATGTATT	NP_001350162.1:n.357+31430_357+31431insTTATTAGATGTATT