Canonical Allele Identifier: CA357956400

Gene: BANK1

Linked Data

• MyVariant Identifiers: chr4:g.102839305C>G (hg19) ; chr4:g.101918148C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918148C>G , CM000666.2:g.101918148C>G	GRCh38
NC_000004.11:g.102839305C>G , CM000666.1:g.102839305C>G	GRCh37
NC_000004.10:g.103058328C>G	NCBI36
NG_015824.1:g.132542C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1165C>G MANE Select	ENSP00000320509.4:p.His389Asp
ENST00000322953.8:c.1165C>G	ENSP00000320509.4:p.His389Asp
ENST00000428908.5:c.766C>G	ENSP00000412748.1:p.His256Asp
ENST00000444316.2:c.1075C>G	ENSP00000388817.2:p.His359Asp
ENST00000504592.5:c.1120C>G	ENSP00000421443.1:p.His374Asp
ENST00000508653.5:c.766C>G	ENSP00000422314.1:p.His256Asp
NM_001083907.2:c.1075C>G	NP_001077376.2:p.His359Asp
NM_001127507.2:c.766C>G	NP_001120979.2:p.His256Asp
NM_017935.4:c.1165C>G	NP_060405.4:p.His389Asp
XM_017008337.2:c.1075C>G	XP_016863826.1:p.His359Asp
NM_017935.5:c.1165C>G MANE Select	NP_060405.5:p.His389Asp
NM_001083907.3:c.1075C>G	NP_001077376.3:p.His359Asp
NM_001127507.3:c.766C>G	NP_001120979.3:p.His256Asp