Canonical Allele Identifier: CA10639701
Community Standard Title: NM_003860.4(BANF1):c.*120T>A
Gene: BANF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66003892T>A , CM000673.2:g.66003892T>A GRCh38
NC_000011.9:g.65771363T>A , CM000673.1:g.65771363T>A GRCh37
NC_000011.8:g.65527939T>A NCBI36
NG_031874.1:g.6814T>A

Transcript Alleles

HGVS Amino-acid Change
NM_003860.4:c.*120T>A MANE Select NP_003851.1:n.*120T>A
ENST00000312175.7:c.*120T>A MANE Select ENSP00000310275.2:n.*120T>A
NM_001143985.1:c.*120T>A NP_001137457.1:n.*120T>A
NM_003860.3:c.*120T>A NP_003851.1:n.*120T>A
ENST00000312175.6:c.*120T>A ENSP00000310275.2:n.*120T>A
ENST00000445560.6:c.*120T>A ENSP00000416128.2:n.*120T>A
ENST00000524628.1:n.358T>A
ENST00000527348.1:c.*120T>A ENSP00000432867.1:n.*120T>A
ENST00000528648.1:n.361T>A
ENST00000533166.5:c.*120T>A ENSP00000433760.1:n.*120T>A
XM_017018514.1:c.*120T>A XP_016874003.1:n.*120T>A
XM_017018515.2:c.*120T>A XP_016874004.1:n.*120T>A