Canonical Allele Identifier: CA1066075827
Gene: BANK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101818885_101818890dup , CM000666.2:g.101818885_101818890dup GRCh38
NC_000004.11:g.102740042_102740047dup , CM000666.1:g.102740042_102740047dup GRCh37
NC_000004.10:g.102959065_102959070dup NCBI36
NG_015824.1:g.33279_33284dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000322953.9:c.71-10923_71-10918dup MANE Select ENSP00000320509.4:n.71-10923_71-10918dup
ENST00000322953.8:c.71-10923_71-10918dup ENSP00000320509.4:n.71-10923_71-10918dup
ENST00000428908.5:c.70+27935_70+27940dup ENSP00000412748.1:n.70+27935_70+27940dup
ENST00000444316.2:c.-21+4947_-21+4952dup ENSP00000388817.2:n.-21+4947_-21+4952dup
ENST00000504592.5:c.26-10923_26-10918dup ENSP00000421443.1:n.26-10923_26-10918dup
ENST00000508653.5:c.70+27935_70+27940dup ENSP00000422314.1:n.70+27935_70+27940dup
NM_001083907.2:c.-21+4947_-21+4952dup NP_001077376.2:n.-21+4947_-21+4952dup
NM_001127507.2:c.70+27935_70+27940dup NP_001120979.2:n.70+27935_70+27940dup
NM_017935.4:c.71-10923_71-10918dup NP_060405.4:n.71-10923_71-10918dup
XM_017008337.2:c.-20-10923_-20-10918dup XP_016863826.1:n.-20-10923_-20-10918dup
NM_017935.5:c.71-10923_71-10918dup MANE Select NP_060405.5:n.71-10923_71-10918dup
NM_001083907.3:c.-21+4947_-21+4952dup NP_001077376.3:n.-21+4947_-21+4952dup
NM_001127507.3:c.70+27935_70+27940dup NP_001120979.3:n.70+27935_70+27940dup