Canonical Allele Identifier: CA363652604

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33575345C>G , CM000668.2:g.33575345C>G GRCh38
NC_000006.11:g.33543122C>G , CM000668.1:g.33543122C>G GRCh37
NC_000006.10:g.33651100C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374467.4:c.303G>C (BAK1) MANE Select ENSP00000363591.3:p.Gln101His
ENST00000360661.9:c.243G>C (BAK1) ENSP00000353878.6:p.Gln81His
ENST00000374467.3:c.303G>C (BAK1) ENSP00000363591.3:p.Gln101His
ENST00000442998.6:c.303G>C (BAK1) ENSP00000391258.2:p.Gln101His
ENST00000612409.1:n.249-6C>G (GGNBP1)
NM_001188.3:c.303G>C (BAK1) NP_001179.1:p.Gln101His
XM_011514779.1:c.303G>C (BAK1) XP_011513081.1:p.Gln101His
XM_011514780.1:c.126G>C (BAK1) XP_011513082.1:p.Gln42His
XM_011514779.3:c.303G>C (BAK1) XP_011513081.1:p.Gln101His
NM_001188.4:c.303G>C (BAK1) MANE Select NP_001179.1:p.Gln101His