Canonical Allele Identifier: CA1481090034

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101818601C= , CM000666.2:g.101818601C=	GRCh38
NC_000004.11:g.102739758C= , CM000666.1:g.102739758C=	GRCh37
NC_000004.10:g.102958781C=	NCBI36
NG_015824.1:g.32995C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.71-11207C= MANE Select	ENSP00000320509.4:n.71-11207C=
ENST00000322953.8:c.71-11207C=	ENSP00000320509.4:n.71-11207C=
ENST00000428908.5:c.70+27651C=	ENSP00000412748.1:n.70+27651C=
ENST00000444316.2:c.-21+4663C=	ENSP00000388817.2:n.-21+4663C=
ENST00000504592.5:c.26-11207C=	ENSP00000421443.1:n.26-11207C=
ENST00000508653.5:c.70+27651C=	ENSP00000422314.1:n.70+27651C=
NM_001083907.2:c.-21+4663C=	NP_001077376.2:n.-21+4663C=
NM_001127507.2:c.70+27651C=	NP_001120979.2:n.70+27651C=
NM_017935.4:c.71-11207C=	NP_060405.4:n.71-11207C=
XM_017008337.2:c.-20-11207C=	XP_016863826.1:n.-20-11207C=
NM_017935.5:c.71-11207C= MANE Select	NP_060405.5:n.71-11207C=
NM_001083907.3:c.-21+4663C=	NP_001077376.3:n.-21+4663C=
NM_001127507.3:c.70+27651C=	NP_001120979.3:n.70+27651C=