Canonical Allele Identifier: CA394570412
Community Standard Title: NM_004380.3(CREBBP):c.3235C>T (p.Gln1079Ter)
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3767735G>A , CM000678.2:g.3767735G>A GRCh38
NC_000016.9:g.3817736G>A , CM000678.1:g.3817736G>A GRCh37
NC_000016.8:g.3757737G>A NCBI36
NG_009873.1:g.117386C>T
NG_009873.2:g.117979C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004380.3:c.3235C>T MANE Select NP_004371.2:p.Gln1079Ter
ENST00000262367.10:c.3235C>T MANE Select ENSP00000262367.5:p.Gln1079Ter
NM_001079846.1:c.3121C>T NP_001073315.1:p.Gln1041Ter
NM_004380.2:c.3235C>T NP_004371.2:p.Gln1079Ter
ENST00000262367.9:c.3235C>T ENSP00000262367.5:p.Gln1079Ter
ENST00000382070.7:c.3121C>T ENSP00000371502.3:p.Gln1041Ter
ENST00000570939.2:c.1840C>T ENSP00000461002.2:p.Gln614Ter
ENST00000573672.1:n.489C>T
XM_005255124.3:c.3190C>T XP_005255181.1:p.Gln1064Ter
XM_005255124.4:c.3190C>T XP_005255181.1:p.Gln1064Ter
XM_005255125.3:c.2818C>T XP_005255182.1:p.Gln940Ter
XM_005255125.4:c.2818C>T XP_005255182.1:p.Gln940Ter
XM_006720848.2:c.3235C>T XP_006720911.1:p.Gln1079Ter
XM_006720848.3:c.3235C>T XP_006720911.1:p.Gln1079Ter
XM_011522380.1:c.3181C>T XP_011520682.1:p.Gln1061Ter
XM_011522381.1:c.2482C>T XP_011520683.1:p.Gln828Ter
XM_011522381.2:c.2482C>T XP_011520683.1:p.Gln828Ter
XM_011522382.1:c.3235C>T XP_011520684.1:p.Gln1079Ter
XM_011522382.3:c.3235C>T XP_011520684.1:p.Gln1079Ter
XM_017022944.1:c.3229C>T XP_016878433.1:p.Gln1077Ter