Canonical Allele Identifier: CA1481095035

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829919G= , CM000666.2:g.101829919G=	GRCh38
NC_000004.11:g.102751076G= , CM000666.1:g.102751076G=	GRCh37
NC_000004.10:g.102970099G=	NCBI36
NG_015824.1:g.44313G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.182G= MANE Select	ENSP00000320509.4:p.Arg61=
ENST00000322953.8:c.182G=	ENSP00000320509.4:p.Arg61=
ENST00000428908.5:c.71-25116G=	ENSP00000412748.1:n.71-25116G=
ENST00000444316.2:c.92G=	ENSP00000388817.2:p.Arg31=
ENST00000504592.5:c.137G=	ENSP00000421443.1:p.Arg46=
ENST00000508653.5:c.71-25116G=	ENSP00000422314.1:n.71-25116G=
NM_001083907.2:c.92G=	NP_001077376.2:p.Arg31=
NM_001127507.2:c.71-25116G=	NP_001120979.2:n.71-25116G=
NM_017935.4:c.182G=	NP_060405.4:p.Arg61=
XM_017008337.2:c.92G=	XP_016863826.1:p.Arg31=
NM_017935.5:c.182G= MANE Select	NP_060405.5:p.Arg61=
NM_001083907.3:c.92G=	NP_001077376.3:p.Arg31=
NM_001127507.3:c.71-25116G=	NP_001120979.3:n.71-25116G=