Canonical Allele Identifier: CA16620203
Gene: CREBBP HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3731244C>G , CM000678.2:g.3731244C>G GRCh38
NC_000016.9:g.3781245C>G , CM000678.1:g.3781245C>G GRCh37
NC_000016.8:g.3721246C>G NCBI36
NG_009873.1:g.153877G>C
NG_009873.2:g.154470G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5120G>C MANE Select ENSP00000262367.5:p.Cys1707Ser
ENST00000637492.1:c.7G>C
ENST00000262367.9:c.5120G>C ENSP00000262367.5:p.Cys1707Ser
ENST00000382070.7:c.5006G>C ENSP00000371502.3:p.Cys1669Ser
NM_001079846.1:c.5006G>C NP_001073315.1:p.Cys1669Ser
NM_004380.2:c.5120G>C NP_004371.2:p.Cys1707Ser
XM_005255124.3:c.5075G>C XP_005255181.1:p.Cys1692Ser
XM_005255125.3:c.4703G>C XP_005255182.1:p.Cys1568Ser
XM_006720848.2:c.4859G>C XP_006720911.1:p.Cys1620Ser
XM_011522380.1:c.5066G>C XP_011520682.1:p.Cys1689Ser
XM_011522381.1:c.4367G>C XP_011520683.1:p.Cys1456Ser
XM_005255124.4:c.5075G>C XP_005255181.1:p.Cys1692Ser
XM_005255125.4:c.4703G>C XP_005255182.1:p.Cys1568Ser
XM_006720848.3:c.4859G>C XP_006720911.1:p.Cys1620Ser
XM_011522381.2:c.4367G>C XP_011520683.1:p.Cys1456Ser
XM_017022944.1:c.5114G>C XP_016878433.1:p.Cys1705Ser
NM_004380.3:c.5120G>C MANE Select NP_004371.2:p.Cys1707Ser