Canonical Allele Identifier: CA2241365075

Gene: CBFA2T3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88897893G= , CM000678.2:g.88897893G=	GRCh38
NC_000016.9:g.88964301G= , CM000678.1:g.88964301G=	GRCh37
NC_000016.8:g.87491802G=	NCBI36
NG_029533.1:g.84204C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268679.9:c.379+185C= MANE Select	ENSP00000268679.4:n.379+185C=
ENST00000268679.8:c.379+185C=	ENSP00000268679.4:n.379+185C=
ENST00000327483.9:c.121+3611C=	ENSP00000332122.5:n.121+3611C=
ENST00000562719.5:c.196+185C=	ENSP00000456717.1:n.196+185C=
ENST00000563640.1:c.304+3611C=	ENSP00000454872.1:n.304+3611C=
ENST00000569443.5:c.121+3611C=	ENSP00000457410.1:n.121+3611C=
ENST00000569464.5:c.196+185C=	ENSP00000454851.1:n.196+185C=
NM_005187.5:c.379+185C=	NP_005178.4:n.379+185C=
NM_175931.2:c.121+3611C=	NP_787127.1:n.121+3611C=
XM_005256323.3:c.304+3611C=	XP_005256380.1:n.304+3611C=
XM_006721319.2:c.196+185C=	XP_006721382.1:n.196+185C=
XM_006721320.2:c.196+185C=	XP_006721383.1:n.196+185C=
XM_011523419.1:c.379+185C=	XP_011521721.1:n.379+185C=
XR_933473.1:n.771+185C=
XM_005256323.5:c.304+3611C=	XP_005256380.1:n.304+3611C=
XM_011523419.3:c.379+185C=	XP_011521721.1:n.379+185C=
XM_024450476.1:c.196+185C=	XP_024306244.1:n.196+185C=
XR_002957849.1:n.523+185C=
XR_933473.3:n.523+185C=
NM_005187.6:c.379+185C= MANE Select	NP_005178.4:n.379+185C=
NM_175931.3:c.121+3611C=	NP_787127.1:n.121+3611C=