Canonical Allele Identifier: CA449868025

Linked Data

MyVariant Identifiers: chr6:g.33543119G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33575342G>T , CM000668.2:g.33575342G>T GRCh38
NC_000006.11:g.33543119G>T , CM000668.1:g.33543119G>T GRCh37
NC_000006.10:g.33651097G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000374467.4:c.306C>A (BAK1) MANE Select ENSP00000363591.3:p.Pro102=
ENST00000360661.9:c.246C>A (BAK1) ENSP00000353878.6:p.Pro82=
ENST00000374467.3:c.306C>A (BAK1) ENSP00000363591.3:p.Pro102=
ENST00000442998.6:c.306C>A (BAK1) ENSP00000391258.2:p.Pro102=
ENST00000612409.1:n.249-9G>T (GGNBP1)
NM_001188.3:c.306C>A (BAK1) NP_001179.1:p.Pro102=
XM_011514779.1:c.306C>A (BAK1) XP_011513081.1:p.Pro102=
XM_011514780.1:c.129C>A (BAK1) XP_011513082.1:p.Pro43=
XM_011514779.3:c.306C>A (BAK1) XP_011513081.1:p.Pro102=
NM_001188.4:c.306C>A (BAK1) MANE Select NP_001179.1:p.Pro102=