Canonical Allele Identifier: CA394554030
Gene: CREBBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728888C>G , CM000678.2:g.3728888C>G GRCh38
NC_000016.9:g.3778889C>G , CM000678.1:g.3778889C>G GRCh37
NC_000016.8:g.3718890C>G NCBI36
NG_009873.1:g.156233G>C
NG_009873.2:g.156826G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6159G>C MANE Select ENSP00000262367.5:p.Met2053Ile
ENST00000262367.9:c.6159G>C ENSP00000262367.5:p.Met2053Ile
ENST00000382070.7:c.6045G>C ENSP00000371502.3:p.Met2015Ile
NM_001079846.1:c.6045G>C NP_001073315.1:p.Met2015Ile
NM_004380.2:c.6159G>C NP_004371.2:p.Met2053Ile
XM_005255124.3:c.6114G>C XP_005255181.1:p.Met2038Ile
XM_005255125.3:c.5742G>C XP_005255182.1:p.Met1914Ile
XM_006720848.2:c.5898G>C XP_006720911.1:p.Met1966Ile
XM_011522380.1:c.6105G>C XP_011520682.1:p.Met2035Ile
XM_011522381.1:c.5406G>C XP_011520683.1:p.Met1802Ile
XM_005255124.4:c.6114G>C XP_005255181.1:p.Met2038Ile
XM_005255125.4:c.5742G>C XP_005255182.1:p.Met1914Ile
XM_006720848.3:c.5898G>C XP_006720911.1:p.Met1966Ile
XM_011522381.2:c.5406G>C XP_011520683.1:p.Met1802Ile
XM_017022944.1:c.6153G>C XP_016878433.1:p.Met2051Ile
NM_004380.3:c.6159G>C MANE Select NP_004371.2:p.Met2053Ile