Canonical Allele Identifier: CA1481094981
Gene: BANK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101829785G= , CM000666.2:g.101829785G= GRCh38
NC_000004.11:g.102750942G= , CM000666.1:g.102750942G= GRCh37
NC_000004.10:g.102969965G= NCBI36
NG_015824.1:g.44179G=

Transcript Alleles

HGVS Amino-acid change
ENST00000322953.9:c.71-23G= MANE Select ENSP00000320509.4:p.=
ENST00000322953.8:c.71-23G= ENSP00000320509.4:p.=
ENST00000428908.5:c.71-25250G= ENSP00000412748.1:p.=
ENST00000444316.2:c.-20-23G= ENSP00000388817.2:p.=
ENST00000504592.5:c.26-23G= ENSP00000421443.1:p.=
ENST00000508653.5:c.71-25250G= ENSP00000422314.1:p.=
NM_001083907.2:c.-20-23G= NP_001077376.2:p.=
NM_001127507.2:c.71-25250G= NP_001120979.2:p.=
NM_017935.4:c.71-23G= NP_060405.4:p.=
XM_017008337.2:c.-20-23G= XP_016863826.1:p.=
NM_017935.5:c.71-23G= MANE Select NP_060405.5:p.=
NM_001083907.3:c.-20-23G= NP_001077376.3:p.=
NM_001127507.3:c.71-25250G= NP_001120979.3:p.=