Canonical Allele Identifier: CA357955728

Gene: BANK1

Linked Data

• MyVariant Identifiers: chr4:g.102839165A>T (hg19) ; chr4:g.101918008A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918008A>T , CM000666.2:g.101918008A>T	GRCh38
NC_000004.11:g.102839165A>T , CM000666.1:g.102839165A>T	GRCh37
NC_000004.10:g.103058188A>T	NCBI36
NG_015824.1:g.132402A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.1025A>T MANE Select	ENSP00000320509.4:p.Glu342Val
ENST00000322953.8:c.1025A>T	ENSP00000320509.4:p.Glu342Val
ENST00000428908.5:c.626A>T	ENSP00000412748.1:p.Glu209Val
ENST00000444316.2:c.935A>T	ENSP00000388817.2:p.Glu312Val
ENST00000504592.5:c.980A>T	ENSP00000421443.1:p.Glu327Val
ENST00000508653.5:c.626A>T	ENSP00000422314.1:p.Glu209Val
NM_001083907.2:c.935A>T	NP_001077376.2:p.Glu312Val
NM_001127507.2:c.626A>T	NP_001120979.2:p.Glu209Val
NM_017935.4:c.1025A>T	NP_060405.4:p.Glu342Val
XM_017008337.2:c.935A>T	XP_016863826.1:p.Glu312Val
NM_017935.5:c.1025A>T MANE Select	NP_060405.5:p.Glu342Val
NM_001083907.3:c.935A>T	NP_001077376.3:p.Glu312Val
NM_001127507.3:c.626A>T	NP_001120979.3:p.Glu209Val