Canonical Allele Identifier: CA1139661704
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119670136_119670137insGCG , CM000672.2:g.119670136_119670137insGCG GRCh38
NC_000010.10:g.121429648_121429649insGCG , CM000672.1:g.121429648_121429649insGCG GRCh37
NC_000010.9:g.121419638_121419639insGCG NCBI36
NG_016125.1:g.23767_23768insGCG , LRG_742:g.23767_23768insGCG

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.466_467insGCG MANE Select ENSP00000358081.4:p.Ala155_Ala156insGly
ENST00000369085.7:c.466_467insGCG ENSP00000358081.3:p.Ala155_Ala156insGly
ENST00000450186.1:c.292_293insGCG ENSP00000410036.1:p.Ala97_Ala98insGly
NM_004281.3:c.466_467insGCG , LRG_742t1:c.466_467insGCG NP_004272.2:p.Ala155_Ala156insGly
XM_005270287.1:c.466_467insGCG XP_005270344.1:p.Ala155_Ala156insGly
XM_005270287.2:c.466_467insGCG XP_005270344.1:p.Ala155_Ala156insGly
NM_004281.4:c.466_467insGCG MANE Select NP_004272.2:p.Ala155_Ala156insGly