Canonical Allele Identifier: CA1620075394

Linked Data

dbSNP Id: rs210142

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33579060T>A , CM000668.2:g.33579060T>A GRCh38
NC_000006.11:g.33546837T>A , CM000668.1:g.33546837T>A GRCh37
NC_000006.10:g.33654815T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374467.4:c.-32+965A>T (BAK1) MANE Select ENSP00000363591.3:n.-32+965A>T
ENST00000360661.9:c.-32+965A>T (BAK1) ENSP00000353878.6:n.-32+965A>T
ENST00000374467.3:c.-32+965A>T (BAK1) ENSP00000363591.3:n.-32+965A>T
ENST00000442998.6:c.-32+965A>T (BAK1) ENSP00000391258.2:n.-32+965A>T
ENST00000612409.1:n.362+3596T>A (GGNBP1)
NM_001188.3:c.-32+965A>T (BAK1) NP_001179.1:n.-32+965A>T
XM_011514779.1:c.-143+965A>T (BAK1) XP_011513081.1:n.-143+965A>T
XM_011514780.1:c.-147+965A>T (BAK1) XP_011513082.1:n.-147+965A>T
XM_011514779.3:c.-143+965A>T (BAK1) XP_011513081.1:n.-143+965A>T
NM_001188.4:c.-32+965A>T (BAK1) MANE Select NP_001179.1:n.-32+965A>T