Canonical Allele Identifier: CA493280348

Gene: CREBBP

Linked Data

• MyVariant Identifiers: chr16:g.3790450C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3740449C>A , CM000678.2:g.3740449C>A	GRCh38
NC_000016.9:g.3790450C>A , CM000678.1:g.3790450C>A	GRCh37
NC_000016.8:g.3730451C>A	NCBI36
NG_009873.1:g.144672G>T
NG_009873.2:g.145265G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.4083G>T MANE Select	ENSP00000262367.5:p.Val1361=
ENST00000262367.9:c.4083G>T	ENSP00000262367.5:p.Val1361=
ENST00000382070.7:c.3969G>T	ENSP00000371502.3:p.Val1323=
ENST00000570939.2:c.2718G>T	ENSP00000461002.2:p.Val906=
ENST00000572569.1:n.547G>T
ENST00000573517.6:c.389G>T
ENST00000574740.1:n.165G>T
ENST00000576720.1:n.3020G>T
NM_001079846.1:c.3969G>T	NP_001073315.1:p.Val1323=
NM_004380.2:c.4083G>T	NP_004371.2:p.Val1361=
XM_005255124.3:c.4038G>T	XP_005255181.1:p.Val1346=
XM_005255125.3:c.3666G>T	XP_005255182.1:p.Val1222=
XM_006720848.2:c.4083G>T	XP_006720911.1:p.Val1361=
XM_011522380.1:c.4029G>T	XP_011520682.1:p.Val1343=
XM_011522381.1:c.3330G>T	XP_011520683.1:p.Val1110=
XM_005255124.4:c.4038G>T	XP_005255181.1:p.Val1346=
XM_005255125.4:c.3666G>T	XP_005255182.1:p.Val1222=
XM_006720848.3:c.4083G>T	XP_006720911.1:p.Val1361=
XM_011522381.2:c.3330G>T	XP_011520683.1:p.Val1110=
XM_017022944.1:c.4077G>T	XP_016878433.1:p.Val1359=
NM_004380.3:c.4083G>T MANE Select	NP_004371.2:p.Val1361=