Canonical Allele Identifier: CA1620072207

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33573942A>T , CM000668.2:g.33573942A>T GRCh38
NC_000006.11:g.33541719A>T , CM000668.1:g.33541719A>T GRCh37
NC_000006.10:g.33649697A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000374467.4:c.532-35T>A (BAK1) MANE Select ENSP00000363591.3:n.532-35T>A
ENST00000360661.9:c.472-35T>A (BAK1) ENSP00000353878.6:n.472-35T>A
ENST00000374467.3:c.532-35T>A (BAK1) ENSP00000363591.3:n.532-35T>A
ENST00000442998.6:c.*90-35T>A (BAK1) ENSP00000391258.2:n.*90-35T>A
ENST00000612409.1:n.249-1409A>T (GGNBP1)
NM_001188.3:c.532-35T>A (BAK1) NP_001179.1:n.532-35T>A
XM_011514779.1:c.532-35T>A (BAK1) XP_011513081.1:n.532-35T>A
XM_011514780.1:c.355-35T>A (BAK1) XP_011513082.1:n.355-35T>A
XM_011514779.3:c.532-35T>A (BAK1) XP_011513081.1:n.532-35T>A
NM_001188.4:c.532-35T>A (BAK1) MANE Select NP_001179.1:n.532-35T>A