Canonical Allele Identifier: CA1481094991

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829808G= , CM000666.2:g.101829808G=	GRCh38
NC_000004.11:g.102750965G= , CM000666.1:g.102750965G=	GRCh37
NC_000004.10:g.102969988G=	NCBI36
NG_015824.1:g.44202G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.71G= MANE Select	ENSP00000320509.4:p.Gly24=
ENST00000322953.8:c.71G=	ENSP00000320509.4:p.Gly24=
ENST00000428908.5:c.71-25227G=	ENSP00000412748.1:n.71-25227G=
ENST00000444316.2:c.-20G=	ENSP00000388817.2:n.-20G=
ENST00000504592.5:c.26G=	ENSP00000421443.1:p.Gly9=
ENST00000508653.5:c.71-25227G=	ENSP00000422314.1:n.71-25227G=
NM_001083907.2:c.-20G=	NP_001077376.2:n.-20G=
NM_001127507.2:c.71-25227G=	NP_001120979.2:n.71-25227G=
NM_017935.4:c.71G=	NP_060405.4:p.Gly24=
XM_017008337.2:c.-20G=	XP_016863826.1:n.-20G=
NM_017935.5:c.71G= MANE Select	NP_060405.5:p.Gly24=
NM_001083907.3:c.-20G=	NP_001077376.3:n.-20G=
NM_001127507.3:c.71-25227G=	NP_001120979.3:n.71-25227G=