Canonical Allele Identifier: CA440820466

Gene: BANK1

Linked Data

• gnomAD v4: 4-101829818-A-G
• MyVariant Identifiers: chr4:g.102750975A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101829818A>G , CM000666.2:g.101829818A>G	GRCh38
NC_000004.11:g.102750975A>G , CM000666.1:g.102750975A>G	GRCh37
NC_000004.10:g.102969998A>G	NCBI36
NG_015824.1:g.44212A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.81A>G MANE Select	ENSP00000320509.4:p.Lys27=
ENST00000322953.8:c.81A>G	ENSP00000320509.4:p.Lys27=
ENST00000428908.5:c.71-25217A>G	ENSP00000412748.1:n.71-25217A>G
ENST00000444316.2:c.-10A>G	ENSP00000388817.2:n.-10A>G
ENST00000504592.5:c.36A>G	ENSP00000421443.1:p.Lys12=
ENST00000508653.5:c.71-25217A>G	ENSP00000422314.1:n.71-25217A>G
NM_001083907.2:c.-10A>G	NP_001077376.2:n.-10A>G
NM_001127507.2:c.71-25217A>G	NP_001120979.2:n.71-25217A>G
NM_017935.4:c.81A>G	NP_060405.4:p.Lys27=
XM_017008337.2:c.-10A>G	XP_016863826.1:n.-10A>G
NM_017935.5:c.81A>G MANE Select	NP_060405.5:p.Lys27=
NM_001083907.3:c.-10A>G	NP_001077376.3:n.-10A>G
NM_001127507.3:c.71-25217A>G	NP_001120979.3:n.71-25217A>G