Canonical Allele Identifier: CA1940192907
Gene: BAG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672194_119672195delinsAG , CM000672.2:g.119672194_119672195delinsAG GRCh38
NC_000010.10:g.121431706_121431707delinsAG , CM000672.1:g.121431706_121431707delinsAG GRCh37
NC_000010.9:g.121421696_121421697delinsAG NCBI36
NG_016125.1:g.25825_25826delinsAG , LRG_742:g.25825_25826delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.508-61_508-60delinsAG MANE Select ENSP00000358081.4:n.508-61_508-60delinsAG
ENST00000369085.7:c.508-61_508-60delinsAG ENSP00000358081.3:n.508-61_508-60delinsAG
ENST00000450186.1:c.334-61_334-60delinsAG ENSP00000410036.1:n.334-61_334-60delinsAG
NM_004281.3:c.508-61_508-60delinsAG , LRG_742t1:c.508-61_508-60delinsAG NP_004272.2:n.508-61_508-60delinsAG
XM_005270287.1:c.508-61_508-60delinsAG XP_005270344.1:n.508-61_508-60delinsAG
XM_005270287.2:c.508-61_508-60delinsAG XP_005270344.1:n.508-61_508-60delinsAG
NM_004281.4:c.508-61_508-60delinsAG MANE Select NP_004272.2:n.508-61_508-60delinsAG