Canonical Allele Identifier: CA1940196658
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676714C= , CM000672.2:g.119676714C= GRCh38
NC_000010.10:g.121436226C= , CM000672.1:g.121436226C= GRCh37
NC_000010.9:g.121426216C= NCBI36
NG_016125.1:g.30345C= , LRG_742:g.30345C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.1160C= MANE Select ENSP00000358081.4:p.Pro387=
ENST00000369085.7:c.1160C= ENSP00000358081.3:p.Pro387=
NM_004281.3:c.1160C= , LRG_742t1:c.1160C= NP_004272.2:p.Pro387=
XM_005270287.1:c.1157C= XP_005270344.1:p.Pro386=
XM_005270287.2:c.1157C= XP_005270344.1:p.Pro386=
NM_004281.4:c.1160C= MANE Select NP_004272.2:p.Pro387=