Canonical Allele Identifier: CA2671540492
Gene: BANK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101829824_101829829del , CM000666.2:g.101829824_101829829del GRCh38
NC_000004.11:g.102750981_102750986del , CM000666.1:g.102750981_102750986del GRCh37
NC_000004.10:g.102970004_102970009del NCBI36
NG_015824.1:g.44218_44223del

Transcript Alleles

HGVS Amino-acid change
ENST00000322953.9:c.87_92del MANE Select ENSP00000320509.4:p.Ile29_Ile30del
ENST00000322953.8:c.87_92del ENSP00000320509.4:p.Ile29_Ile30del
ENST00000428908.5:c.71-25211_71-25206del ENSP00000412748.1:n.71-25211_71-25206del
ENST00000444316.2:c.-4_2del ENSP00000388817.2:n.-4_2del
ENST00000504592.5:c.42_47del ENSP00000421443.1:p.Ile14_Ile15del
ENST00000508653.5:c.71-25211_71-25206del ENSP00000422314.1:n.71-25211_71-25206del
NM_001083907.2:c.-4_2del NP_001077376.2:n.-4_2del
NM_001127507.2:c.71-25211_71-25206del NP_001120979.2:n.71-25211_71-25206del
NM_017935.4:c.87_92del NP_060405.4:p.Ile29_Ile30del
XM_017008337.2:c.-4_2del XP_016863826.1:n.-4_2del
NM_017935.5:c.87_92del MANE Select NP_060405.5:p.Ile29_Ile30del
NM_001083907.3:c.-4_2del NP_001077376.3:n.-4_2del
NM_001127507.3:c.71-25211_71-25206del NP_001120979.3:n.71-25211_71-25206del