Canonical Allele Identifier: CA1481138661

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918040T= , CM000666.2:g.101918040T=	GRCh38
NC_000004.11:g.102839197T= , CM000666.1:g.102839197T=	GRCh37
NC_000004.10:g.103058220T=	NCBI36
NG_015824.1:g.132434T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.1057T= MANE Select	ENSP00000320509.4:p.Phe353=
ENST00000322953.8:c.1057T=	ENSP00000320509.4:p.Phe353=
ENST00000428908.5:c.658T=	ENSP00000412748.1:p.Phe220=
ENST00000444316.2:c.967T=	ENSP00000388817.2:p.Phe323=
ENST00000504592.5:c.1012T=	ENSP00000421443.1:p.Phe338=
ENST00000508653.5:c.658T=	ENSP00000422314.1:p.Phe220=
NM_001083907.2:c.967T=	NP_001077376.2:p.Phe323=
NM_001127507.2:c.658T=	NP_001120979.2:p.Phe220=
NM_017935.4:c.1057T=	NP_060405.4:p.Phe353=
XM_017008337.2:c.967T=	XP_016863826.1:p.Phe323=
NM_017935.5:c.1057T= MANE Select	NP_060405.5:p.Phe353=
NM_001083907.3:c.967T=	NP_001077376.3:p.Phe323=
NM_001127507.3:c.658T=	NP_001120979.3:p.Phe220=