Canonical Allele Identifier: CA1481138706

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918132A= , CM000666.2:g.101918132A=	GRCh38
NC_000004.11:g.102839289A= , CM000666.1:g.102839289A=	GRCh37
NC_000004.10:g.103058312A=	NCBI36
NG_015824.1:g.132526A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.1149A= MANE Select	ENSP00000320509.4:p.Ala383=
ENST00000322953.8:c.1149A=	ENSP00000320509.4:p.Ala383=
ENST00000428908.5:c.750A=	ENSP00000412748.1:p.Ala250=
ENST00000444316.2:c.1059A=	ENSP00000388817.2:p.Ala353=
ENST00000504592.5:c.1104A=	ENSP00000421443.1:p.Ala368=
ENST00000508653.5:c.750A=	ENSP00000422314.1:p.Ala250=
NM_001083907.2:c.1059A=	NP_001077376.2:p.Ala353=
NM_001127507.2:c.750A=	NP_001120979.2:p.Ala250=
NM_017935.4:c.1149A=	NP_060405.4:p.Ala383=
XM_017008337.2:c.1059A=	XP_016863826.1:p.Ala353=
NM_017935.5:c.1149A= MANE Select	NP_060405.5:p.Ala383=
NM_001083907.3:c.1059A=	NP_001077376.3:p.Ala353=
NM_001127507.3:c.750A=	NP_001120979.3:p.Ala250=