Canonical Allele Identifier: CA394554829

Gene: CREBBP

Linked Data

• dbSNP Id: rs2141234478
• MyVariant Identifiers: chr16:g.3828150A>T (hg19) ; chr16:g.3778149A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3778149A>T , CM000678.2:g.3778149A>T	GRCh38
NC_000016.9:g.3828150A>T , CM000678.1:g.3828150A>T	GRCh37
NC_000016.8:g.3768151A>T	NCBI36
NG_009873.1:g.106972T>A
NG_009873.2:g.107565T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.1975T>A MANE Select	ENSP00000262367.5:p.Tyr659Asn
ENST00000262367.9:c.1975T>A	ENSP00000262367.5:p.Tyr659Asn
ENST00000382070.7:c.1861T>A	ENSP00000371502.3:p.Tyr621Asn
ENST00000570939.2:c.580T>A	ENSP00000461002.2:p.Tyr194Asn
ENST00000571826.5:c.24T>A
ENST00000572134.1:c.288T>A
ENST00000634839.1:n.137T>A
NM_001079846.1:c.1861T>A	NP_001073315.1:p.Tyr621Asn
NM_004380.2:c.1975T>A	NP_004371.2:p.Tyr659Asn
XM_005255124.3:c.1975T>A	XP_005255181.1:p.Tyr659Asn
XM_005255125.3:c.1975T>A	XP_005255182.1:p.Tyr659Asn
XM_006720848.2:c.1975T>A	XP_006720911.1:p.Tyr659Asn
XM_011522380.1:c.1921T>A	XP_011520682.1:p.Tyr641Asn
XM_011522381.1:c.1222T>A	XP_011520683.1:p.Tyr408Asn
XM_011522382.1:c.1975T>A	XP_011520684.1:p.Tyr659Asn
XM_005255124.4:c.1975T>A	XP_005255181.1:p.Tyr659Asn
XM_005255125.4:c.1975T>A	XP_005255182.1:p.Tyr659Asn
XM_006720848.3:c.1975T>A	XP_006720911.1:p.Tyr659Asn
XM_011522381.2:c.1222T>A	XP_011520683.1:p.Tyr408Asn
XM_011522382.3:c.1975T>A	XP_011520684.1:p.Tyr659Asn
XM_017022944.1:c.1975T>A	XP_016878433.1:p.Tyr659Asn
NM_004380.3:c.1975T>A MANE Select	NP_004371.2:p.Tyr659Asn