Canonical Allele Identifier: CA394553441
Community Standard Title: NM_004380.3(CREBBP):c.2159-1G>T
Gene: CREBBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3774694C>A , CM000678.2:g.3774694C>A GRCh38
NC_000016.9:g.3824695C>A , CM000678.1:g.3824695C>A GRCh37
NC_000016.8:g.3764696C>A NCBI36
NG_009873.1:g.110427G>T
NG_009873.2:g.111020G>T

Transcript Alleles

HGVS Amino-acid Change
NM_004380.3:c.2159-1G>T MANE Select NP_004371.2:n.2159-1G>T
ENST00000262367.10:c.2159-1G>T MANE Select ENSP00000262367.5:n.2159-1G>T
NM_001079846.1:c.2045-1G>T NP_001073315.1:n.2045-1G>T
NM_004380.2:c.2159-1G>T NP_004371.2:n.2159-1G>T
ENST00000262367.9:c.2159-1G>T ENSP00000262367.5:n.2159-1G>T
ENST00000382070.7:c.2045-1G>T ENSP00000371502.3:n.2045-1G>T
ENST00000570939.2:c.764-1G>T ENSP00000461002.2:n.764-1G>T
ENST00000571826.5:c.208-1G>T
ENST00000572134.1:c.427-1G>T
ENST00000575237.2:n.53G>T
XM_005255124.3:c.2114-1G>T XP_005255181.1:n.2114-1G>T
XM_005255124.4:c.2114-1G>T XP_005255181.1:n.2114-1G>T
XM_005255125.3:c.2159-1G>T XP_005255182.1:n.2159-1G>T
XM_005255125.4:c.2159-1G>T XP_005255182.1:n.2159-1G>T
XM_006720848.2:c.2159-1G>T XP_006720911.1:n.2159-1G>T
XM_006720848.3:c.2159-1G>T XP_006720911.1:n.2159-1G>T
XM_011522380.1:c.2105-1G>T XP_011520682.1:n.2105-1G>T
XM_011522381.1:c.1406-1G>T XP_011520683.1:n.1406-1G>T
XM_011522381.2:c.1406-1G>T XP_011520683.1:n.1406-1G>T
XM_011522382.1:c.2159-1G>T XP_011520684.1:n.2159-1G>T
XM_011522382.3:c.2159-1G>T XP_011520684.1:n.2159-1G>T
XM_017022944.1:c.2159-1G>T XP_016878433.1:n.2159-1G>T