Canonical Allele Identifier: CA1770581677
Gene: PEBP4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22786101_22786102delinsAT , CM000670.2:g.22786101_22786102delinsAT GRCh38
NC_000008.10:g.22643614_22643615delinsAT , CM000670.1:g.22643614_22643615delinsAT GRCh37
NC_000008.9:g.22699559_22699560delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256404.8:c.357+31535_357+31536delinsAT MANE Select ENSP00000256404.6:n.357+31535_357+31536de...
ENST00000256404.7:c.357+31535_357+31536delinsAT ENSP00000256404.6:n.357+31535_357+31536de...
NM_144962.2:c.357+31535_357+31536delinsAT NP_659399.2:n.357+31535_357+31536delinsAT...
XM_011544413.1:c.357+31535_357+31536delinsAT XP_011542715.1:n.357+31535_357+31536delin...
XM_011544414.1:c.357+31535_357+31536delinsAT XP_011542716.1:n.357+31535_357+31536delin...
NM_001363233.1:c.357+31535_357+31536delinsAT NP_001350162.1:n.357+31535_357+31536delin...
NM_144962.3:c.357+31535_357+31536delinsAT MANE Select NP_659399.2:n.357+31535_357+31536delinsAT...
NM_001363233.2:c.357+31535_357+31536delinsAT NP_001350162.1:n.357+31535_357+31536delin...
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