Canonical Allele Identifier: CA1620071335
Community Standard Title: NM_001188.4(BAK1):c.*888A=

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33572915T= , CM000668.2:g.33572915T= GRCh38
NC_000006.11:g.33540692T= , CM000668.1:g.33540692T= GRCh37
NC_000006.10:g.33648670T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001188.4:c.*888A= (BAK1) MANE Select NP_001179.1:n.*888A=
ENST00000374467.4:c.*888A= (BAK1) MANE Select ENSP00000363591.3:n.*888A=
NM_001188.3:c.*888A= (BAK1) NP_001179.1:n.*888A=
ENST00000360661.9:c.*888A= (BAK1) ENSP00000353878.6:n.*888A=
ENST00000374467.3:c.*888A= (BAK1) ENSP00000363591.3:n.*888A=
ENST00000442998.6:c.*1082A= (BAK1) ENSP00000391258.2:n.*1082A=
ENST00000612409.1:n.248+2104T= (GGNBP1)
XM_011514779.1:c.*888A= (BAK1) XP_011513081.1:n.*888A=
XM_011514779.3:c.*888A= (BAK1) XP_011513081.1:n.*888A=
XM_011514780.1:c.*888A= (BAK1) XP_011513082.1:n.*888A=