Canonical Allele Identifier: CA378296547
Gene: BAG3 HGNC NCBI

Linked Data

dbSNP Id: rs1564776574

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676609C>T , CM000672.2:g.119676609C>T GRCh38
NC_000010.10:g.121436121C>T , CM000672.1:g.121436121C>T GRCh37
NC_000010.9:g.121426111C>T NCBI36
NG_016125.1:g.30240C>T , LRG_742:g.30240C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1055C>T MANE Select ENSP00000358081.4:p.Ser352Phe
ENST00000369085.7:c.1055C>T ENSP00000358081.3:p.Ser352Phe
ENST00000450186.1:c.878C>T ENSP00000410036.1:p.Ser293Phe
NM_004281.3:c.1055C>T , LRG_742t1:c.1055C>T NP_004272.2:p.Ser352Phe
XM_005270287.1:c.1052C>T XP_005270344.1:p.Ser351Phe
XM_005270287.2:c.1052C>T XP_005270344.1:p.Ser351Phe
NM_004281.4:c.1055C>T MANE Select NP_004272.2:p.Ser352Phe