Canonical Allele Identifier: CA394568597
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3757837T>A , CM000678.2:g.3757837T>A GRCh38
NC_000016.9:g.3807838T>A , CM000678.1:g.3807838T>A GRCh37
NC_000016.8:g.3747839T>A NCBI36
NG_009873.1:g.127284A>T
NG_009873.2:g.127877A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.3581A>T MANE Select ENSP00000262367.5:p.Gln1194Leu
ENST00000262367.9:c.3581A>T ENSP00000262367.5:p.Gln1194Leu
ENST00000382070.7:c.3467A>T ENSP00000371502.3:p.Gln1156Leu
ENST00000570939.2:c.2186A>T ENSP00000461002.2:p.Gln729Leu
NM_001079846.1:c.3467A>T NP_001073315.1:p.Gln1156Leu
NM_004380.2:c.3581A>T NP_004371.2:p.Gln1194Leu
XM_005255124.3:c.3536A>T XP_005255181.1:p.Gln1179Leu
XM_005255125.3:c.3164A>T XP_005255182.1:p.Gln1055Leu
XM_006720848.2:c.3581A>T XP_006720911.1:p.Gln1194Leu
XM_011522380.1:c.3527A>T XP_011520682.1:p.Gln1176Leu
XM_011522381.1:c.2828A>T XP_011520683.1:p.Gln943Leu
XM_011522382.1:c.3581A>T XP_011520684.1:p.Gln1194Leu
XM_005255124.4:c.3536A>T XP_005255181.1:p.Gln1179Leu
XM_005255125.4:c.3164A>T XP_005255182.1:p.Gln1055Leu
XM_006720848.3:c.3581A>T XP_006720911.1:p.Gln1194Leu
XM_011522381.2:c.2828A>T XP_011520683.1:p.Gln943Leu
XM_011522382.3:c.3581A>T XP_011520684.1:p.Gln1194Leu
XM_017022944.1:c.3575A>T XP_016878433.1:p.Gln1192Leu
NM_004380.3:c.3581A>T MANE Select NP_004371.2:p.Gln1194Leu