Canonical Allele Identifier: CA1066075855
Gene: BANK1 HGNC NCBI

Linked Data

dbSNP Id: rs1726026375

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101818890_101818891insTTTTTTTTTTTTTTTTG , CM000666.2:g.101818890_101818891insTTTTTTTTTTTTTTTTG GRCh38
NC_000004.11:g.102740047_102740048insTTTTTTTTTTTTTTTTG , CM000666.1:g.102740047_102740048insTTTTTTTTTTTTTTTTG GRCh37
NC_000004.10:g.102959070_102959071insTTTTTTTTTTTTTTTTG NCBI36
NG_015824.1:g.33284_33285insTTTTTTTTTTTTTTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000322953.9:c.71-10918_71-10917insTTTTTTTTTTTTTTTTG MANE Select ENSP00000320509.4:n.71-10918_71-10917insTTTTTTTTTTTTTTTTG
ENST00000322953.8:c.71-10918_71-10917insTTTTTTTTTTTTTTTTG ENSP00000320509.4:n.71-10918_71-10917insTTTTTTTTTTTTTTTTG
ENST00000428908.5:c.70+27940_70+27941insTTTTTTTTTTTTTTTTG ENSP00000412748.1:n.70+27940_70+27941insTTTTTTTTTTTTTTTTG
ENST00000444316.2:c.-21+4952_-21+4953insTTTTTTTTTTTTTTTTG ENSP00000388817.2:n.-21+4952_-21+4953insTTTTTTTTTTTTTTTTG
ENST00000504592.5:c.26-10918_26-10917insTTTTTTTTTTTTTTTTG ENSP00000421443.1:n.26-10918_26-10917insTTTTTTTTTTTTTTTTG
ENST00000508653.5:c.70+27940_70+27941insTTTTTTTTTTTTTTTTG ENSP00000422314.1:n.70+27940_70+27941insTTTTTTTTTTTTTTTTG
NM_001083907.2:c.-21+4952_-21+4953insTTTTTTTTTTTTTTTTG NP_001077376.2:n.-21+4952_-21+4953insTTTTTTTTTTTTTTTTG
NM_001127507.2:c.70+27940_70+27941insTTTTTTTTTTTTTTTTG NP_001120979.2:n.70+27940_70+27941insTTTTTTTTTTTTTTTTG
NM_017935.4:c.71-10918_71-10917insTTTTTTTTTTTTTTTTG NP_060405.4:n.71-10918_71-10917insTTTTTTTTTTTTTTTTG
XM_017008337.2:c.-20-10918_-20-10917insTTTTTTTTTTTTTTTTG XP_016863826.1:n.-20-10918_-20-10917insTTTTTTTTTTTTTTTTG
NM_017935.5:c.71-10918_71-10917insTTTTTTTTTTTTTTTTG MANE Select NP_060405.5:n.71-10918_71-10917insTTTTTTTTTTTTTTTTG
NM_001083907.3:c.-21+4952_-21+4953insTTTTTTTTTTTTTTTTG NP_001077376.3:n.-21+4952_-21+4953insTTTTTTTTTTTTTTTTG
NM_001127507.3:c.70+27940_70+27941insTTTTTTTTTTTTTTTTG NP_001120979.3:n.70+27940_70+27941insTTTTTTTTTTTTTTTTG