Canonical Allele Identifier: CA1139662024
Community Standard Title: NM_003860.4(BANF1):c.*143T>A
Gene: BANF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66003915T>A , CM000673.2:g.66003915T>A GRCh38
NC_000011.9:g.65771386T>A , CM000673.1:g.65771386T>A GRCh37
NC_000011.8:g.65527962T>A NCBI36
NG_031874.1:g.6837T>A

Transcript Alleles

HGVS Amino-acid Change
NM_003860.4:c.*143T>A MANE Select NP_003851.1:n.*143T>A
ENST00000312175.7:c.*143T>A MANE Select ENSP00000310275.2:n.*143T>A
NM_001143985.1:c.*143T>A NP_001137457.1:n.*143T>A
NM_003860.3:c.*143T>A NP_003851.1:n.*143T>A
ENST00000312175.6:c.*143T>A ENSP00000310275.2:n.*143T>A
ENST00000445560.6:c.*143T>A ENSP00000416128.2:n.*143T>A
ENST00000524628.1:n.381T>A
ENST00000533166.5:c.*143T>A ENSP00000433760.1:n.*143T>A
XM_017018514.1:c.*143T>A XP_016874003.1:n.*143T>A
XM_017018515.2:c.*143T>A XP_016874004.1:n.*143T>A