Canonical Allele Identifier: CA1481090023
Gene: BANK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101818577T= , CM000666.2:g.101818577T= GRCh38
NC_000004.11:g.102739734T= , CM000666.1:g.102739734T= GRCh37
NC_000004.10:g.102958757T= NCBI36
NG_015824.1:g.32971T=

Transcript Alleles

HGVS Amino-acid change
ENST00000322953.9:c.71-11231T= MANE Select ENSP00000320509.4:n.71-11231T=
ENST00000322953.8:c.71-11231T= ENSP00000320509.4:n.71-11231T=
ENST00000428908.5:c.70+27627T= ENSP00000412748.1:n.70+27627T=
ENST00000444316.2:c.-21+4639T= ENSP00000388817.2:n.-21+4639T=
ENST00000504592.5:c.26-11231T= ENSP00000421443.1:n.26-11231T=
ENST00000508653.5:c.70+27627T= ENSP00000422314.1:n.70+27627T=
NM_001083907.2:c.-21+4639T= NP_001077376.2:n.-21+4639T=
NM_001127507.2:c.70+27627T= NP_001120979.2:n.70+27627T=
NM_017935.4:c.71-11231T= NP_060405.4:n.71-11231T=
XM_017008337.2:c.-20-11231T= XP_016863826.1:n.-20-11231T=
NM_017935.5:c.71-11231T= MANE Select NP_060405.5:n.71-11231T=
NM_001083907.3:c.-21+4639T= NP_001077376.3:n.-21+4639T=
NM_001127507.3:c.70+27627T= NP_001120979.3:n.70+27627T=