Canonical Allele Identifier: CA1481138709

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918139G= , CM000666.2:g.101918139G=	GRCh38
NC_000004.11:g.102839296G= , CM000666.1:g.102839296G=	GRCh37
NC_000004.10:g.103058319G=	NCBI36
NG_015824.1:g.132533G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.1156G= MANE Select	ENSP00000320509.4:p.Ala386=
ENST00000322953.8:c.1156G=	ENSP00000320509.4:p.Ala386=
ENST00000428908.5:c.757G=	ENSP00000412748.1:p.Ala253=
ENST00000444316.2:c.1066G=	ENSP00000388817.2:p.Ala356=
ENST00000504592.5:c.1111G=	ENSP00000421443.1:p.Ala371=
ENST00000508653.5:c.757G=	ENSP00000422314.1:p.Ala253=
NM_001083907.2:c.1066G=	NP_001077376.2:p.Ala356=
NM_001127507.2:c.757G=	NP_001120979.2:p.Ala253=
NM_017935.4:c.1156G=	NP_060405.4:p.Ala386=
XM_017008337.2:c.1066G=	XP_016863826.1:p.Ala356=
NM_017935.5:c.1156G= MANE Select	NP_060405.5:p.Ala386=
NM_001083907.3:c.1066G=	NP_001077376.3:p.Ala356=
NM_001127507.3:c.757G=	NP_001120979.3:p.Ala253=