Canonical Allele Identifier: CA1619251072
Gene: C6orf47 HGNC NCBI
BAG6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31658303C= , CM000668.2:g.31658303C= GRCh38
NC_000006.11:g.31626080C= , CM000668.1:g.31626080C= GRCh37
NC_000006.10:g.31734059C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375911.2:c.*760G= (C6orf47) MANE Select ENSP00000365076.1:n.*760G=
ENST00000375911.1:c.*760G= (C6orf47) ENSP00000365076.1:n.*760G=
NM_021184.3:c.*760G= (C6orf47) NP_067007.3:n.*760G=
XM_011514895.1:c.-14+2018G= (BAG6) XP_011513197.1:n.-14+2018G=
XM_017011279.2:c.-14+2018G= (BAG6) XP_016866768.1:n.-14+2018G=
NM_021184.4:c.*760G= (C6orf47) MANE Select NP_067007.3:n.*760G=