Canonical Allele Identifier: CA1940196715
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119676819_119676829delinsTGCTGAAAGTG , CM000672.2:g.119676819_119676829delinsTGCTGAAAGTG GRCh38
NC_000010.10:g.121436331_121436341delinsTGCTGAAAGTG , CM000672.1:g.121436331_121436341delinsTGCTGAAAGTG GRCh37
NC_000010.9:g.121426321_121426331delinsTGCTGAAAGTG NCBI36
NG_016125.1:g.30450_30460delinsTGCTGAAAGTG , LRG_742:g.30450_30460delinsTGCTGAAAGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000369085.8:c.1265_1275delinsTGCTGAAAGTG MANE Select ENSP00000358081.4:p.Val422=
ENST00000369085.7:c.1265_1275delinsTGCTGAAAGTG ENSP00000358081.3:p.Val422=
NM_004281.3:c.1265_1275delinsTGCTGAAAGTG , LRG_742t1:c.1265_1275delinsTGCTGAAAGTG NP_004272.2:p.Val422=
XM_005270287.1:c.1262_1272delinsTGCTGAAAGTG XP_005270344.1:p.Val421=
XM_005270287.2:c.1262_1272delinsTGCTGAAAGTG XP_005270344.1:p.Val421=
NM_004281.4:c.1265_1275delinsTGCTGAAAGTG MANE Select NP_004272.2:p.Val422=