Canonical Allele Identifier: CA6114070
Community Standard Title: NM_003860.4(BANF1):c.9C>T (p.Thr3=)
Gene: BANF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66003259C>T , CM000673.2:g.66003259C>T GRCh38
NC_000011.9:g.65770730C>T , CM000673.1:g.65770730C>T GRCh37
NC_000011.8:g.65527306C>T NCBI36
NG_031874.1:g.6181C>T

Transcript Alleles

HGVS Amino-acid Change
NM_003860.4:c.9C>T MANE Select NP_003851.1:p.Thr3=
ENST00000312175.7:c.9C>T MANE Select ENSP00000310275.2:p.Thr3=
NM_001143985.1:c.9C>T NP_001137457.1:p.Thr3=
NM_003860.3:c.9C>T NP_003851.1:p.Thr3=
ENST00000312175.6:c.9C>T ENSP00000310275.2:p.Thr3=
ENST00000445560.6:c.9C>T ENSP00000416128.2:p.Thr3=
ENST00000524628.1:n.92-367C>T
ENST00000524663.1:n.199-367C>T
ENST00000527348.1:c.9C>T ENSP00000432867.1:p.Thr3=
ENST00000528648.1:n.24C>T
ENST00000530204.1:c.9C>T ENSP00000431785.1:p.Thr3=
ENST00000533166.5:c.9C>T ENSP00000433760.1:p.Thr3=
XM_017018514.1:c.9C>T XP_016874003.1:p.Thr3=
XM_017018515.2:c.9C>T XP_016874004.1:p.Thr3=