Canonical Allele Identifier: CA824059526

Genomic Alleles

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

Transcript Alleles

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