Canonical Allele Identifier: CA1481088896

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101816027G= , CM000666.2:g.101816027G=	GRCh38
NC_000004.11:g.102737184G= , CM000666.1:g.102737184G=	GRCh37
NC_000004.10:g.102956207G=	NCBI36
NG_015824.1:g.30421G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.71-13781G= MANE Select	ENSP00000320509.4:n.71-13781G=
ENST00000322953.8:c.71-13781G=	ENSP00000320509.4:n.71-13781G=
ENST00000428908.5:c.70+25077G=	ENSP00000412748.1:n.70+25077G=
ENST00000444316.2:c.-21+2089G=	ENSP00000388817.2:n.-21+2089G=
ENST00000504592.5:c.26-13781G=	ENSP00000421443.1:n.26-13781G=
ENST00000508653.5:c.70+25077G=	ENSP00000422314.1:n.70+25077G=
NM_001083907.2:c.-21+2089G=	NP_001077376.2:n.-21+2089G=
NM_001127507.2:c.70+25077G=	NP_001120979.2:n.70+25077G=
NM_017935.4:c.71-13781G=	NP_060405.4:n.71-13781G=
XM_017008337.2:c.-20-13781G=	XP_016863826.1:n.-20-13781G=
NM_017935.5:c.71-13781G= MANE Select	NP_060405.5:n.71-13781G=
NM_001083907.3:c.-21+2089G=	NP_001077376.3:n.-21+2089G=
NM_001127507.3:c.70+25077G=	NP_001120979.3:n.70+25077G=