Canonical Allele Identifier: CA1481132277

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101944096G= , CM000666.2:g.101944096G=	GRCh38
NC_000004.11:g.102865253G= , CM000666.1:g.102865253G=	GRCh37
NC_000004.10:g.103084276G=	NCBI36
NG_015824.1:g.158490G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1206+25907G= MANE Select	ENSP00000320509.4:n.1206+25907G=
ENST00000322953.8:c.1206+25907G=	ENSP00000320509.4:n.1206+25907G=
ENST00000428908.5:c.807+25907G=	ENSP00000412748.1:n.807+25907G=
ENST00000444316.2:c.1116+25907G=	ENSP00000388817.2:n.1116+25907G=
ENST00000504592.5:c.1161+25907G=	ENSP00000421443.1:n.1161+25907G=
ENST00000508653.5:c.807+25907G=	ENSP00000422314.1:n.807+25907G=
NM_001083907.2:c.1116+25907G=	NP_001077376.2:n.1116+25907G=
NM_001127507.2:c.807+25907G=	NP_001120979.2:n.807+25907G=
NM_017935.4:c.1206+25907G=	NP_060405.4:n.1206+25907G=
XM_017008337.2:c.1116+25907G=	XP_016863826.1:n.1116+25907G=
NM_017935.5:c.1206+25907G= MANE Select	NP_060405.5:n.1206+25907G=
NM_001083907.3:c.1116+25907G=	NP_001077376.3:n.1116+25907G=
NM_001127507.3:c.807+25907G=	NP_001120979.3:n.807+25907G=