Canonical Allele Identifier: CA440606646

Gene: BANK1

Linked Data

• MyVariant Identifiers: chr4:g.102839310T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918153T>G , CM000666.2:g.101918153T>G	GRCh38
NC_000004.11:g.102839310T>G , CM000666.1:g.102839310T>G	GRCh37
NC_000004.10:g.103058333T>G	NCBI36
NG_015824.1:g.132547T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.1170T>G MANE Select	ENSP00000320509.4:p.Gly390=
ENST00000322953.8:c.1170T>G	ENSP00000320509.4:p.Gly390=
ENST00000428908.5:c.771T>G	ENSP00000412748.1:p.Gly257=
ENST00000444316.2:c.1080T>G	ENSP00000388817.2:p.Gly360=
ENST00000504592.5:c.1125T>G	ENSP00000421443.1:p.Gly375=
ENST00000508653.5:c.771T>G	ENSP00000422314.1:p.Gly257=
NM_001083907.2:c.1080T>G	NP_001077376.2:p.Gly360=
NM_001127507.2:c.771T>G	NP_001120979.2:p.Gly257=
NM_017935.4:c.1170T>G	NP_060405.4:p.Gly390=
XM_017008337.2:c.1080T>G	XP_016863826.1:p.Gly360=
NM_017935.5:c.1170T>G MANE Select	NP_060405.5:p.Gly390=
NM_001083907.3:c.1080T>G	NP_001077376.3:p.Gly360=
NM_001127507.3:c.771T>G	NP_001120979.3:p.Gly257=