Canonical Allele Identifier: CA2830546205

Gene: BAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.33262513del , CM000671.2:g.33262513del	GRCh38
NC_000009.11:g.33262511del , CM000671.1:g.33262511del	GRCh37
NC_000009.10:g.33252511del	NCBI36
NG_029018.1:g.7250del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634734.3:c.580+190del MANE Select	ENSP00000489189.2:n.580+190del
ENST00000379704.7:c.235+190del	ENSP00000369026.2:n.235+190del
ENST00000379707.7:c.235+190del	ENSP00000369029.2:n.235+190del
ENST00000472232.7:c.580+190del	ENSP00000420514.3:n.580+190del
ENST00000473781.1:c.253+190del	ENSP00000419092.1:n.253+190del
ENST00000634734.1:c.580+190del	ENSP00000489189.1:n.580+190del
ENST00000635077.1:c.253+190del	ENSP00000488937.1:n.253+190del
NM_001172415.1:c.235+190del	NP_001165886.1:n.235+190del
NM_004323.5:c.580+190del	NP_004314.5:n.580+190del
NM_001349286.1:c.367+190del	NP_001336215.1:n.367+190del
NM_001349299.1:c.166+190del	NP_001336228.1:n.166+190del
NM_004323.6:c.580+190del MANE Select	NP_004314.6:n.580+190del
NM_001172415.2:c.235+190del	NP_001165886.1:n.235+190del
NM_001349286.2:c.367+190del	NP_001336215.1:n.367+190del
NM_001349299.2:c.166+190del	NP_001336228.1:n.166+190del