Canonical Allele Identifier: CA493280075
Gene: CREBBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.3789587T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3739586T>C , CM000678.2:g.3739586T>C GRCh38
NC_000016.9:g.3789587T>C , CM000678.1:g.3789587T>C GRCh37
NC_000016.8:g.3729588T>C NCBI36
NG_009873.1:g.145535A>G
NG_009873.2:g.146128A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4272A>G MANE Select ENSP00000262367.5:p.Pro1424=
ENST00000262367.9:c.4272A>G ENSP00000262367.5:p.Pro1424=
ENST00000382070.7:c.4158A>G ENSP00000371502.3:p.Pro1386=
ENST00000570939.2:c.2907A>G ENSP00000461002.2:p.Pro969=
ENST00000573517.6:c.578A>G
ENST00000574740.1:n.215+813A>G
ENST00000576720.1:n.3209A>G
NM_001079846.1:c.4158A>G NP_001073315.1:p.Pro1386=
NM_004380.2:c.4272A>G NP_004371.2:p.Pro1424=
XM_005255124.3:c.4227A>G XP_005255181.1:p.Pro1409=
XM_005255125.3:c.3855A>G XP_005255182.1:p.Pro1285=
XM_006720848.2:c.4133+813A>G XP_006720911.1:n.4133+813A>G
XM_011522380.1:c.4218A>G XP_011520682.1:p.Pro1406=
XM_011522381.1:c.3519A>G XP_011520683.1:p.Pro1173=
XM_005255124.4:c.4227A>G XP_005255181.1:p.Pro1409=
XM_005255125.4:c.3855A>G XP_005255182.1:p.Pro1285=
XM_006720848.3:c.4133+813A>G XP_006720911.1:n.4133+813A>G
XM_011522381.2:c.3519A>G XP_011520683.1:p.Pro1173=
XM_017022944.1:c.4266A>G XP_016878433.1:p.Pro1422=
NM_004380.3:c.4272A>G MANE Select NP_004371.2:p.Pro1424=