Canonical Allele Identifier: CA1940192912
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672199G= , CM000672.2:g.119672199G= GRCh38
NC_000010.10:g.121431711G= , CM000672.1:g.121431711G= GRCh37
NC_000010.9:g.121421701G= NCBI36
NG_016125.1:g.25830G= , LRG_742:g.25830G=

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.508-56G= MANE Select ENSP00000358081.4:n.508-56G=
ENST00000369085.7:c.508-56G= ENSP00000358081.3:n.508-56G=
ENST00000450186.1:c.334-56G= ENSP00000410036.1:n.334-56G=
NM_004281.3:c.508-56G= , LRG_742t1:c.508-56G= NP_004272.2:n.508-56G=
XM_005270287.1:c.508-56G= XP_005270344.1:n.508-56G=
XM_005270287.2:c.508-56G= XP_005270344.1:n.508-56G=
NM_004281.4:c.508-56G= MANE Select NP_004272.2:n.508-56G=