Canonical Allele Identifier: CA363652656

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33575352T>C , CM000668.2:g.33575352T>C GRCh38
NC_000006.11:g.33543129T>C , CM000668.1:g.33543129T>C GRCh37
NC_000006.10:g.33651107T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000374467.4:c.296A>G (BAK1) MANE Select ENSP00000363591.3:p.His99Arg
ENST00000360661.9:c.236A>G (BAK1) ENSP00000353878.6:p.His79Arg
ENST00000374467.3:c.296A>G (BAK1) ENSP00000363591.3:p.His99Arg
ENST00000442998.6:c.296A>G (BAK1) ENSP00000391258.2:p.His99Arg
ENST00000612409.1:n.250T>C (GGNBP1)
NM_001188.3:c.296A>G (BAK1) NP_001179.1:p.His99Arg
XM_011514779.1:c.296A>G (BAK1) XP_011513081.1:p.His99Arg
XM_011514780.1:c.119A>G (BAK1) XP_011513082.1:p.His40Arg
XM_011514779.3:c.296A>G (BAK1) XP_011513081.1:p.His99Arg
NM_001188.4:c.296A>G (BAK1) MANE Select NP_001179.1:p.His99Arg