Canonical Allele Identifier: CA357956412

Gene: BANK1

Linked Data

• MyVariant Identifiers: chr4:g.102839311C>T (hg19) ; chr4:g.101918154C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918154C>T , CM000666.2:g.101918154C>T	GRCh38
NC_000004.11:g.102839311C>T , CM000666.1:g.102839311C>T	GRCh37
NC_000004.10:g.103058334C>T	NCBI36
NG_015824.1:g.132548C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000322953.9:c.1171C>T MANE Select	ENSP00000320509.4:p.His391Tyr
ENST00000322953.8:c.1171C>T	ENSP00000320509.4:p.His391Tyr
ENST00000428908.5:c.772C>T	ENSP00000412748.1:p.His258Tyr
ENST00000444316.2:c.1081C>T	ENSP00000388817.2:p.His361Tyr
ENST00000504592.5:c.1126C>T	ENSP00000421443.1:p.His376Tyr
ENST00000508653.5:c.772C>T	ENSP00000422314.1:p.His258Tyr
NM_001083907.2:c.1081C>T	NP_001077376.2:p.His361Tyr
NM_001127507.2:c.772C>T	NP_001120979.2:p.His258Tyr
NM_017935.4:c.1171C>T	NP_060405.4:p.His391Tyr
XM_017008337.2:c.1081C>T	XP_016863826.1:p.His361Tyr
NM_017935.5:c.1171C>T MANE Select	NP_060405.5:p.His391Tyr
NM_001083907.3:c.1081C>T	NP_001077376.3:p.His361Tyr
NM_001127507.3:c.772C>T	NP_001120979.3:p.His258Tyr