Canonical Allele Identifier: CA1979481978

Gene: BANF1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66003284G= , CM000673.2:g.66003284G=	GRCh38
NC_000011.9:g.65770755G= , CM000673.1:g.65770755G=	GRCh37
NC_000011.8:g.65527331G=	NCBI36
NG_031874.1:g.6206G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312175.7:c.34G= MANE Select	ENSP00000310275.2:p.Ala12=
ENST00000312175.6:c.34G=	ENSP00000310275.2:p.Ala12=
ENST00000445560.6:c.34G=	ENSP00000416128.2:p.Ala12=
ENST00000524628.1:n.92-342G=
ENST00000524663.1:n.199-342G=
ENST00000527348.1:c.34G=	ENSP00000432867.1:p.Ala12=
ENST00000528648.1:n.49G=
ENST00000530204.1:c.34G=	ENSP00000431785.1:p.Ala12=
ENST00000533166.5:c.34G=	ENSP00000433760.1:p.Ala12=
NM_001143985.1:c.34G=	NP_001137457.1:p.Ala12=
NM_003860.3:c.34G=	NP_003851.1:p.Ala12=
XM_017018514.1:c.34G=	XP_016874003.1:p.Ala12=
XM_017018515.2:c.34G=	XP_016874004.1:p.Ala12=
NM_003860.4:c.34G= MANE Select	NP_003851.1:p.Ala12=