Canonical Allele Identifier: CA394553580

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3778698G>A (hg19) ; chr16:g.3728697G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728697G>A , CM000678.2:g.3728697G>A	GRCh38
NC_000016.9:g.3778698G>A , CM000678.1:g.3778698G>A	GRCh37
NC_000016.8:g.3718699G>A	NCBI36
NG_009873.1:g.156424C>T
NG_009873.2:g.157017C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6350C>T MANE Select	ENSP00000262367.5:p.Pro2117Leu
ENST00000262367.9:c.6350C>T	ENSP00000262367.5:p.Pro2117Leu
ENST00000382070.7:c.6236C>T	ENSP00000371502.3:p.Pro2079Leu
NM_001079846.1:c.6236C>T	NP_001073315.1:p.Pro2079Leu
NM_004380.2:c.6350C>T	NP_004371.2:p.Pro2117Leu
XM_005255124.3:c.6305C>T	XP_005255181.1:p.Pro2102Leu
XM_005255125.3:c.5933C>T	XP_005255182.1:p.Pro1978Leu
XM_006720848.2:c.6089C>T	XP_006720911.1:p.Pro2030Leu
XM_011522380.1:c.6296C>T	XP_011520682.1:p.Pro2099Leu
XM_011522381.1:c.5597C>T	XP_011520683.1:p.Pro1866Leu
XM_005255124.4:c.6305C>T	XP_005255181.1:p.Pro2102Leu
XM_005255125.4:c.5933C>T	XP_005255182.1:p.Pro1978Leu
XM_006720848.3:c.6089C>T	XP_006720911.1:p.Pro2030Leu
XM_011522381.2:c.5597C>T	XP_011520683.1:p.Pro1866Leu
XM_017022944.1:c.6344C>T	XP_016878433.1:p.Pro2115Leu
NM_004380.3:c.6350C>T MANE Select	NP_004371.2:p.Pro2117Leu