Canonical Allele Identifier: CA1696888429

Gene: CREB5

Linked Data

• dbSNP Id: rs1583616367

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.28723370C>T , CM000669.2:g.28723370C>T	GRCh38
NC_000007.13:g.28762987C>T , CM000669.1:g.28762987C>T	GRCh37
NC_000007.12:g.28729512C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357727.7:c.592-852C>T MANE Select	ENSP00000350359.2:n.592-852C>T
ENST00000357727.6:c.592-852C>T	ENSP00000350359.2:n.592-852C>T
ENST00000396298.6:c.175-852C>T	ENSP00000379592.2:n.175-852C>T
ENST00000396299.6:c.493-852C>T	ENSP00000379593.2:n.493-852C>T
ENST00000396300.6:c.571-852C>T	ENSP00000379594.2:n.571-852C>T
ENST00000409603.5:c.493-852C>T	ENSP00000387197.1:n.493-852C>T
ENST00000426500.5:c.70-852C>T	ENSP00000394979.1:n.70-852C>T
ENST00000461921.5:n.228-852C>T
ENST00000468391.5:n.189-852C>T
ENST00000484383.1:n.189-852C>T
NM_001011666.2:c.175-852C>T	NP_001011666.1:n.175-852C>T
NM_004904.3:c.571-852C>T	NP_004895.2:n.571-852C>T
NM_182898.3:c.592-852C>T	NP_878901.2:n.592-852C>T
NM_182899.4:c.493-852C>T	NP_878902.2:n.493-852C>T
XM_005249906.1:c.571-852C>T	XP_005249963.1:n.571-852C>T
XM_011515616.1:c.571-852C>T	XP_011513918.1:n.571-852C>T
XM_011515617.1:c.493-852C>T	XP_011513919.1:n.493-852C>T
XM_017012806.1:c.571-852C>T	XP_016868295.1:n.571-852C>T
XM_017012807.1:c.679-852C>T	XP_016868296.1:n.679-852C>T
XM_017012808.1:c.592-852C>T	XP_016868297.1:n.592-852C>T
XM_017012809.1:c.571-852C>T	XP_016868298.1:n.571-852C>T
XM_017012810.1:c.175-852C>T	XP_016868299.1:n.175-852C>T
XM_024447005.1:c.493-852C>T	XP_024302773.1:n.493-852C>T
XR_001744893.2:n.364-852C>T
NM_182898.4:c.592-852C>T MANE Select	NP_878901.2:n.592-852C>T
NM_001011666.3:c.175-852C>T	NP_001011666.1:n.175-852C>T
NM_004904.4:c.571-852C>T	NP_004895.2:n.571-852C>T
NM_182899.5:c.493-852C>T	NP_878902.2:n.493-852C>T