Canonical Allele Identifier: CA1770581574

Gene: PEBP4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22786025_22786029delinsAAGAC , CM000670.2:g.22786025_22786029delinsAAGAC	GRCh38
NC_000008.10:g.22643538_22643542delinsAAGAC , CM000670.1:g.22643538_22643542delinsAAGAC	GRCh37
NC_000008.9:g.22699483_22699487delinsAAGAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256404.8:c.357+31608_357+31612delinsGTCTT MANE Select	ENSP00000256404.6:n.357+31608_357+31612delinsGTCTT
ENST00000256404.7:c.357+31608_357+31612delinsGTCTT	ENSP00000256404.6:n.357+31608_357+31612delinsGTCTT
NM_144962.2:c.357+31608_357+31612delinsGTCTT	NP_659399.2:n.357+31608_357+31612delinsGTCTT
XM_011544413.1:c.357+31608_357+31612delinsGTCTT	XP_011542715.1:n.357+31608_357+31612delinsGTCTT
XM_011544414.1:c.357+31608_357+31612delinsGTCTT	XP_011542716.1:n.357+31608_357+31612delinsGTCTT
NM_001363233.1:c.357+31608_357+31612delinsGTCTT	NP_001350162.1:n.357+31608_357+31612delinsGTCTT
NM_144962.3:c.357+31608_357+31612delinsGTCTT MANE Select	NP_659399.2:n.357+31608_357+31612delinsGTCTT
NM_001363233.2:c.357+31608_357+31612delinsGTCTT	NP_001350162.1:n.357+31608_357+31612delinsGTCTT