Canonical Allele Identifier: CA440606642

Gene: BANK1

Linked Data

• gnomAD v4: 4-101918144-A-G
• MyVariant Identifiers: chr4:g.102839301A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918144A>G , CM000666.2:g.101918144A>G	GRCh38
NC_000004.11:g.102839301A>G , CM000666.1:g.102839301A>G	GRCh37
NC_000004.10:g.103058324A>G	NCBI36
NG_015824.1:g.132538A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1161A>G MANE Select	ENSP00000320509.4:p.Glu387=
ENST00000322953.8:c.1161A>G	ENSP00000320509.4:p.Glu387=
ENST00000428908.5:c.762A>G	ENSP00000412748.1:p.Glu254=
ENST00000444316.2:c.1071A>G	ENSP00000388817.2:p.Glu357=
ENST00000504592.5:c.1116A>G	ENSP00000421443.1:p.Glu372=
ENST00000508653.5:c.762A>G	ENSP00000422314.1:p.Glu254=
NM_001083907.2:c.1071A>G	NP_001077376.2:p.Glu357=
NM_001127507.2:c.762A>G	NP_001120979.2:p.Glu254=
NM_017935.4:c.1161A>G	NP_060405.4:p.Glu387=
XM_017008337.2:c.1071A>G	XP_016863826.1:p.Glu357=
NM_017935.5:c.1161A>G MANE Select	NP_060405.5:p.Glu387=
NM_001083907.3:c.1071A>G	NP_001077376.3:p.Glu357=
NM_001127507.3:c.762A>G	NP_001120979.3:p.Glu254=