Canonical Allele Identifier: CA1481088892

Gene: BANK1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101816015T= , CM000666.2:g.101816015T=	GRCh38
NC_000004.11:g.102737172T= , CM000666.1:g.102737172T=	GRCh37
NC_000004.10:g.102956195T=	NCBI36
NG_015824.1:g.30409T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.71-13793T= MANE Select	ENSP00000320509.4:n.71-13793T=
ENST00000322953.8:c.71-13793T=	ENSP00000320509.4:n.71-13793T=
ENST00000428908.5:c.70+25065T=	ENSP00000412748.1:n.70+25065T=
ENST00000444316.2:c.-21+2077T=	ENSP00000388817.2:n.-21+2077T=
ENST00000504592.5:c.26-13793T=	ENSP00000421443.1:n.26-13793T=
ENST00000508653.5:c.70+25065T=	ENSP00000422314.1:n.70+25065T=
NM_001083907.2:c.-21+2077T=	NP_001077376.2:n.-21+2077T=
NM_001127507.2:c.70+25065T=	NP_001120979.2:n.70+25065T=
NM_017935.4:c.71-13793T=	NP_060405.4:n.71-13793T=
XM_017008337.2:c.-20-13793T=	XP_016863826.1:n.-20-13793T=
NM_017935.5:c.71-13793T= MANE Select	NP_060405.5:n.71-13793T=
NM_001083907.3:c.-21+2077T=	NP_001077376.3:n.-21+2077T=
NM_001127507.3:c.70+25065T=	NP_001120979.3:n.70+25065T=