Canonical Allele Identifier: CA440820448

Gene: BANK1

Linked Data

• MyVariant Identifiers: chr4:g.102750966A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829809A>C , CM000666.2:g.101829809A>C	GRCh38
NC_000004.11:g.102750966A>C , CM000666.1:g.102750966A>C	GRCh37
NC_000004.10:g.102969989A>C	NCBI36
NG_015824.1:g.44203A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.72A>C MANE Select	ENSP00000320509.4:p.Gly24=
ENST00000322953.8:c.72A>C	ENSP00000320509.4:p.Gly24=
ENST00000428908.5:c.71-25226A>C	ENSP00000412748.1:n.71-25226A>C
ENST00000444316.2:c.-19A>C	ENSP00000388817.2:n.-19A>C
ENST00000504592.5:c.27A>C	ENSP00000421443.1:p.Gly9=
ENST00000508653.5:c.71-25226A>C	ENSP00000422314.1:n.71-25226A>C
NM_001083907.2:c.-19A>C	NP_001077376.2:n.-19A>C
NM_001127507.2:c.71-25226A>C	NP_001120979.2:n.71-25226A>C
NM_017935.4:c.72A>C	NP_060405.4:p.Gly24=
XM_017008337.2:c.-19A>C	XP_016863826.1:n.-19A>C
NM_017935.5:c.72A>C MANE Select	NP_060405.5:p.Gly24=
NM_001083907.3:c.-19A>C	NP_001077376.3:n.-19A>C
NM_001127507.3:c.71-25226A>C	NP_001120979.3:n.71-25226A>C