Canonical Allele Identifier: CA1620075238

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33578721C= , CM000668.2:g.33578721C= GRCh38
NC_000006.11:g.33546498C= , CM000668.1:g.33546498C= GRCh37
NC_000006.10:g.33654476C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000374467.4:c.-31-1086G= (BAK1) MANE Select ENSP00000363591.3:n.-31-1086G=
ENST00000360661.9:c.-31-1086G= (BAK1) ENSP00000353878.6:n.-31-1086G=
ENST00000374467.3:c.-31-1086G= (BAK1) ENSP00000363591.3:n.-31-1086G=
ENST00000442998.6:c.-31-1086G= (BAK1) ENSP00000391258.2:n.-31-1086G=
ENST00000612409.1:n.362+3257C= (GGNBP1)
NM_001188.3:c.-31-1086G= (BAK1) NP_001179.1:n.-31-1086G=
XM_011514779.1:c.-142-813G= (BAK1) XP_011513081.1:n.-142-813G=
XM_011514780.1:c.-146-1086G= (BAK1) XP_011513082.1:n.-146-1086G=
XM_011514779.3:c.-142-813G= (BAK1) XP_011513081.1:n.-142-813G=
NM_001188.4:c.-31-1086G= (BAK1) MANE Select NP_001179.1:n.-31-1086G=