Canonical Allele Identifier: CA2838278362

Gene: PREB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27131565C>A , CM000664.2:g.27131565C>A	GRCh38
NC_000002.11:g.27354433C>A , CM000664.1:g.27354433C>A	GRCh37
NC_000002.10:g.27207937C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260643.7:c.1160-57G>T MANE Select	ENSP00000260643.2:n.1160-57G>T
ENST00000260643.6:c.1160-57G>T	ENSP00000260643.2:n.1160-57G>T
ENST00000406567.7:c.986-57G>T	ENSP00000384032.3:n.986-57G>T
ENST00000430533.1:c.266-57G>T
ENST00000441451.1:c.283-57G>T	ENSP00000391894.1:n.283-57G>T
ENST00000444452.5:c.*940-57G>T	ENSP00000416103.1:n.*940-57G>T
ENST00000456259.5:c.388-57G>T
ENST00000468045.5:n.2305-57G>T
NM_013388.4:c.1160-57G>T	NP_037520.1:n.1160-57G>T
XM_006711914.2:c.986-57G>T	XP_006711977.1:n.986-57G>T
XM_011532471.1:c.1000-57G>T	XP_011530773.1:n.1000-57G>T
XM_011532472.1:c.826-57G>T	XP_011530774.1:n.826-57G>T
XR_939648.1:n.1420-57G>T
XR_939649.1:n.1260-57G>T
NM_001330484.1:c.944-57G>T	NP_001317413.1:n.944-57G>T
NM_001330485.1:c.986-57G>T	NP_001317414.1:n.986-57G>T
NM_001330486.1:c.1000-57G>T	NP_001317415.1:n.1000-57G>T
NM_001330487.1:c.826-57G>T	NP_001317416.1:n.826-57G>T
NM_013388.5:c.1160-57G>T	NP_037520.1:n.1160-57G>T
NR_138479.1:n.1440-57G>T
XR_939649.3:n.1247-57G>T
NM_013388.6:c.1160-57G>T MANE Select	NP_037520.1:n.1160-57G>T
NM_001330484.2:c.944-57G>T	NP_001317413.1:n.944-57G>T
NM_001330485.2:c.986-57G>T	NP_001317414.1:n.986-57G>T
NM_001330486.2:c.1000-57G>T	NP_001317415.1:n.1000-57G>T
NM_001330487.2:c.826-57G>T	NP_001317416.1:n.826-57G>T
NR_138479.2:n.1401-57G>T