Canonical Allele Identifier: CA357955979

Gene: BANK1

Linked Data

• MyVariant Identifiers: chr4:g.102839211C>A (hg19) ; chr4:g.101918054C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101918054C>A , CM000666.2:g.101918054C>A	GRCh38
NC_000004.11:g.102839211C>A , CM000666.1:g.102839211C>A	GRCh37
NC_000004.10:g.103058234C>A	NCBI36
NG_015824.1:g.132448C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000322953.9:c.1071C>A MANE Select	ENSP00000320509.4:p.Asn357Lys
ENST00000322953.8:c.1071C>A	ENSP00000320509.4:p.Asn357Lys
ENST00000428908.5:c.672C>A	ENSP00000412748.1:p.Asn224Lys
ENST00000444316.2:c.981C>A	ENSP00000388817.2:p.Asn327Lys
ENST00000504592.5:c.1026C>A	ENSP00000421443.1:p.Asn342Lys
ENST00000508653.5:c.672C>A	ENSP00000422314.1:p.Asn224Lys
NM_001083907.2:c.981C>A	NP_001077376.2:p.Asn327Lys
NM_001127507.2:c.672C>A	NP_001120979.2:p.Asn224Lys
NM_017935.4:c.1071C>A	NP_060405.4:p.Asn357Lys
XM_017008337.2:c.981C>A	XP_016863826.1:p.Asn327Lys
NM_017935.5:c.1071C>A MANE Select	NP_060405.5:p.Asn357Lys
NM_001083907.3:c.981C>A	NP_001077376.3:p.Asn327Lys
NM_001127507.3:c.672C>A	NP_001120979.3:p.Asn224Lys