Canonical Allele Identifier: CA1481094979
Gene: BANK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101829780T= , CM000666.2:g.101829780T= GRCh38
NC_000004.11:g.102750937T= , CM000666.1:g.102750937T= GRCh37
NC_000004.10:g.102969960T= NCBI36
NG_015824.1:g.44174T=

Transcript Alleles

HGVS Amino-acid change
ENST00000322953.9:c.71-28T= MANE Select ENSP00000320509.4:p.=
ENST00000322953.8:c.71-28T= ENSP00000320509.4:p.=
ENST00000428908.5:c.71-25255T= ENSP00000412748.1:p.=
ENST00000444316.2:c.-20-28T= ENSP00000388817.2:p.=
ENST00000504592.5:c.26-28T= ENSP00000421443.1:p.=
ENST00000508653.5:c.71-25255T= ENSP00000422314.1:p.=
NM_001083907.2:c.-20-28T= NP_001077376.2:p.=
NM_001127507.2:c.71-25255T= NP_001120979.2:p.=
NM_017935.4:c.71-28T= NP_060405.4:p.=
XM_017008337.2:c.-20-28T= XP_016863826.1:p.=
NM_017935.5:c.71-28T= MANE Select NP_060405.5:p.=
NM_001083907.3:c.-20-28T= NP_001077376.3:p.=
NM_001127507.3:c.71-25255T= NP_001120979.3:p.=