Canonical Allele Identifier: CA1620073700

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33575346T= , CM000668.2:g.33575346T= GRCh38
NC_000006.11:g.33543123T= , CM000668.1:g.33543123T= GRCh37
NC_000006.10:g.33651101T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000374467.4:c.302A= (BAK1) MANE Select ENSP00000363591.3:p.Gln101=
ENST00000360661.9:c.242A= (BAK1) ENSP00000353878.6:p.Gln81=
ENST00000374467.3:c.302A= (BAK1) ENSP00000363591.3:p.Gln101=
ENST00000442998.6:c.302A= (BAK1) ENSP00000391258.2:p.Gln101=
ENST00000612409.1:n.249-5T= (GGNBP1)
NM_001188.3:c.302A= (BAK1) NP_001179.1:p.Gln101=
XM_011514779.1:c.302A= (BAK1) XP_011513081.1:p.Gln101=
XM_011514780.1:c.125A= (BAK1) XP_011513082.1:p.Gln42=
XM_011514779.3:c.302A= (BAK1) XP_011513081.1:p.Gln101=
NM_001188.4:c.302A= (BAK1) MANE Select NP_001179.1:p.Gln101=