Canonical Allele Identifier: CA493279261
Gene: CREBBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.3786702G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736701G>A , CM000678.2:g.3736701G>A GRCh38
NC_000016.9:g.3786702G>A , CM000678.1:g.3786702G>A GRCh37
NC_000016.8:g.3726703G>A NCBI36
NG_009873.1:g.148420C>T
NG_009873.2:g.149013C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4509C>T MANE Select ENSP00000262367.5:p.Tyr1503=
ENST00000262367.9:c.4509C>T ENSP00000262367.5:p.Tyr1503=
ENST00000382070.7:c.4395C>T ENSP00000371502.3:p.Tyr1465=
ENST00000570939.2:c.3144C>T ENSP00000461002.2:p.Tyr1048=
ENST00000571763.5:n.299C>T
ENST00000574740.1:n.330C>T
ENST00000576720.1:n.3332C>T
NM_001079846.1:c.4395C>T NP_001073315.1:p.Tyr1465=
NM_004380.2:c.4509C>T NP_004371.2:p.Tyr1503=
XM_005255124.3:c.4464C>T XP_005255181.1:p.Tyr1488=
XM_005255125.3:c.4092C>T XP_005255182.1:p.Tyr1364=
XM_006720848.2:c.4248C>T XP_006720911.1:p.Tyr1416=
XM_011522380.1:c.4455C>T XP_011520682.1:p.Tyr1485=
XM_011522381.1:c.3756C>T XP_011520683.1:p.Tyr1252=
XM_005255124.4:c.4464C>T XP_005255181.1:p.Tyr1488=
XM_005255125.4:c.4092C>T XP_005255182.1:p.Tyr1364=
XM_006720848.3:c.4248C>T XP_006720911.1:p.Tyr1416=
XM_011522381.2:c.3756C>T XP_011520683.1:p.Tyr1252=
XM_017022944.1:c.4503C>T XP_016878433.1:p.Tyr1501=
NM_004380.3:c.4509C>T MANE Select NP_004371.2:p.Tyr1503=