Canonical Allele Identifier: CA394568760

Gene: CREBBP

Linked Data

• COSMIC: COSM3988469
• MyVariant Identifiers: chr16:g.3807907G>A (hg19) ; chr16:g.3757906G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3757906G>A , CM000678.2:g.3757906G>A	GRCh38
NC_000016.9:g.3807907G>A , CM000678.1:g.3807907G>A	GRCh37
NC_000016.8:g.3747908G>A	NCBI36
NG_009873.1:g.127215C>T
NG_009873.2:g.127808C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.3512C>T MANE Select	ENSP00000262367.5:p.Thr1171Ile
ENST00000262367.9:c.3512C>T	ENSP00000262367.5:p.Thr1171Ile
ENST00000382070.7:c.3398C>T	ENSP00000371502.3:p.Thr1133Ile
ENST00000570939.2:c.2117C>T	ENSP00000461002.2:p.Thr706Ile
NM_001079846.1:c.3398C>T	NP_001073315.1:p.Thr1133Ile
NM_004380.2:c.3512C>T	NP_004371.2:p.Thr1171Ile
XM_005255124.3:c.3467C>T	XP_005255181.1:p.Thr1156Ile
XM_005255125.3:c.3095C>T	XP_005255182.1:p.Thr1032Ile
XM_006720848.2:c.3512C>T	XP_006720911.1:p.Thr1171Ile
XM_011522380.1:c.3458C>T	XP_011520682.1:p.Thr1153Ile
XM_011522381.1:c.2759C>T	XP_011520683.1:p.Thr920Ile
XM_011522382.1:c.3512C>T	XP_011520684.1:p.Thr1171Ile
XM_005255124.4:c.3467C>T	XP_005255181.1:p.Thr1156Ile
XM_005255125.4:c.3095C>T	XP_005255182.1:p.Thr1032Ile
XM_006720848.3:c.3512C>T	XP_006720911.1:p.Thr1171Ile
XM_011522381.2:c.2759C>T	XP_011520683.1:p.Thr920Ile
XM_011522382.3:c.3512C>T	XP_011520684.1:p.Thr1171Ile
XM_017022944.1:c.3506C>T	XP_016878433.1:p.Thr1169Ile
NM_004380.3:c.3512C>T MANE Select	NP_004371.2:p.Thr1171Ile