Canonical Allele Identifier: CA1940192915
Gene: BAG3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119672202_119672206delinsAAGCC , CM000672.2:g.119672202_119672206delinsAAGCC GRCh38
NC_000010.10:g.121431714_121431718delinsAAGCC , CM000672.1:g.121431714_121431718delinsAAGCC GRCh37
NC_000010.9:g.121421704_121421708delinsAAGCC NCBI36
NG_016125.1:g.25833_25837delinsAAGCC , LRG_742:g.25833_25837delinsAAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369085.8:c.508-53_508-49delinsAAGCC MANE Select ENSP00000358081.4:n.508-53_508-49delinsAAGCC
ENST00000369085.7:c.508-53_508-49delinsAAGCC ENSP00000358081.3:n.508-53_508-49delinsAAGCC
ENST00000450186.1:c.334-53_334-49delinsAAGCC ENSP00000410036.1:n.334-53_334-49delinsAAGCC
NM_004281.3:c.508-53_508-49delinsAAGCC , LRG_742t1:c.508-53_508-49delinsAAGCC NP_004272.2:n.508-53_508-49delinsAAGCC
XM_005270287.1:c.508-53_508-49delinsAAGCC XP_005270344.1:n.508-53_508-49delinsAAGCC
XM_005270287.2:c.508-53_508-49delinsAAGCC XP_005270344.1:n.508-53_508-49delinsAAGCC
NM_004281.4:c.508-53_508-49delinsAAGCC MANE Select NP_004272.2:n.508-53_508-49delinsAAGCC
Search 100 bp 5'
Search 100 bp 3'