Canonical Allele Identifier: CA1940192909

Gene: BAG3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119672198_119672204delinsTGCCAAG , CM000672.2:g.119672198_119672204delinsTGCCAAG	GRCh38
NC_000010.10:g.121431710_121431716delinsTGCCAAG , CM000672.1:g.121431710_121431716delinsTGCCAAG	GRCh37
NC_000010.9:g.121421700_121421706delinsTGCCAAG	NCBI36
NG_016125.1:g.25829_25835delinsTGCCAAG , LRG_742:g.25829_25835delinsTGCCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369085.8:c.508-57_508-51delinsTGCCAAG MANE Select	ENSP00000358081.4:n.508-57_508-51delinsTGCCAAG
ENST00000369085.7:c.508-57_508-51delinsTGCCAAG	ENSP00000358081.3:n.508-57_508-51delinsTGCCAAG
ENST00000450186.1:c.334-57_334-51delinsTGCCAAG	ENSP00000410036.1:n.334-57_334-51delinsTGCCAAG
NM_004281.3:c.508-57_508-51delinsTGCCAAG , LRG_742t1:c.508-57_508-51delinsTGCCAAG	NP_004272.2:n.508-57_508-51delinsTGCCAAG
XM_005270287.1:c.508-57_508-51delinsTGCCAAG	XP_005270344.1:n.508-57_508-51delinsTGCCAAG
XM_005270287.2:c.508-57_508-51delinsTGCCAAG	XP_005270344.1:n.508-57_508-51delinsTGCCAAG
NM_004281.4:c.508-57_508-51delinsTGCCAAG MANE Select	NP_004272.2:n.508-57_508-51delinsTGCCAAG