Canonical Allele Identifier: CA1481088952
Gene: BANK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101816156T= , CM000666.2:g.101816156T= GRCh38
NC_000004.11:g.102737313T= , CM000666.1:g.102737313T= GRCh37
NC_000004.10:g.102956336T= NCBI36
NG_015824.1:g.30550T=

Transcript Alleles

HGVS Amino-acid change
ENST00000322953.9:c.71-13652T= MANE Select ENSP00000320509.4:n.71-13652T=
ENST00000322953.8:c.71-13652T= ENSP00000320509.4:n.71-13652T=
ENST00000428908.5:c.70+25206T= ENSP00000412748.1:n.70+25206T=
ENST00000444316.2:c.-21+2218T= ENSP00000388817.2:n.-21+2218T=
ENST00000504592.5:c.26-13652T= ENSP00000421443.1:n.26-13652T=
ENST00000508653.5:c.70+25206T= ENSP00000422314.1:n.70+25206T=
NM_001083907.2:c.-21+2218T= NP_001077376.2:n.-21+2218T=
NM_001127507.2:c.70+25206T= NP_001120979.2:n.70+25206T=
NM_017935.4:c.71-13652T= NP_060405.4:n.71-13652T=
XM_017008337.2:c.-20-13652T= XP_016863826.1:n.-20-13652T=
NM_017935.5:c.71-13652T= MANE Select NP_060405.5:n.71-13652T=
NM_001083907.3:c.-21+2218T= NP_001077376.3:n.-21+2218T=
NM_001127507.3:c.70+25206T= NP_001120979.3:n.70+25206T=