Canonical Allele Identifier: CA3717679
Gene: BAG6 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10484558

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31647737T>C , CM000668.2:g.31647737T>C GRCh38
NC_000006.11:g.31615514T>C , CM000668.1:g.31615514T>C GRCh37
NC_000006.10:g.31723493T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001098534.1:c.642A>G VV NP_001092004.1:p.Thr214=
NM_001199697.1:c.642A>G VV NP_001186626.1:p.Thr214=
NM_001199698.1:c.642A>G VV NP_001186627.1:p.Thr214=
NM_004639.3:c.660A>G VV NP_004630.3:p.Thr220=
NM_080702.2:c.642A>G VV NP_542433.1:p.Thr214=
NM_080703.2:c.642A>G VV NP_542434.1:p.Thr214=
XM_006715192.1:c.642A>G XP_006715255.1:p.Thr214=
XM_006715198.1:c.642A>G XP_006715261.1:p.Thr214=
XM_006715201.1:c.642A>G XP_006715264.1:p.Thr214=
XM_006715203.1:c.642A>G XP_006715266.1:p.Thr214=
XM_011514891.1:c.642A>G XP_011513193.1:p.Thr214=
XM_011514892.1:c.642A>G XP_011513194.1:p.Thr214=
XM_011514893.1:c.642A>G XP_011513195.1:p.Thr214=
XM_011514894.1:c.642A>G XP_011513196.1:p.Thr214=
XM_011514895.1:c.642A>G XP_011513197.1:p.Thr214=
XM_011514896.1:c.642A>G XP_011513198.1:p.Thr214=
XM_011514897.1:c.642A>G XP_011513199.1:p.Thr214=
XM_011514898.1:c.642A>G XP_011513200.1:p.Thr214=
XM_011514899.1:c.588A>G XP_011513201.1:p.Thr196=
XM_011514900.1:c.588A>G XP_011513202.1:p.Thr196=
XM_011514901.1:c.588A>G XP_011513203.1:p.Thr196=
XM_011514902.1:c.642A>G XP_011513204.1:p.Thr214=
XM_011514903.1:c.642A>G XP_011513205.1:p.Thr214=
XM_011514904.1:c.588A>G XP_011513206.1:p.Thr196=
XM_011514905.1:c.642A>G XP_011513207.1:p.Thr214=
XM_011514906.1:c.642A>G XP_011513208.1:p.Thr214=
XM_011514907.1:c.642A>G XP_011513209.1:p.Thr214=
XM_011514908.1:c.588A>G XP_011513210.1:p.Thr196=
XM_011514892.3:c.642A>G
XM_017011275.2:c.642A>G XP_016866764.1:p.Thr214=
XM_017011276.2:c.642A>G XP_016866765.1:p.Thr214=
XM_017011277.2:c.642A>G XP_016866766.1:p.Thr214=
XM_017011278.2:c.642A>G XP_016866767.1:p.Thr214=
XM_017011279.2:c.642A>G XP_016866768.1:p.Thr214=
XM_017011280.2:c.642A>G XP_016866769.1:p.Thr214=
XM_017011281.2:c.642A>G XP_016866770.1:p.Thr214=
XM_017011282.2:c.642A>G XP_016866771.1:p.Thr214=
XM_017011283.2:c.642A>G XP_016866772.1:p.Thr214=
XM_017011284.2:c.642A>G XP_016866773.1:p.Thr214=
XM_017011285.2:c.588A>G XP_016866774.1:p.Thr196=
XM_017011286.2:c.588A>G XP_016866775.1:p.Thr196=
XM_017011287.2:c.642A>G XP_016866776.1:p.Thr214=
XM_017011289.2:c.642A>G XP_016866778.1:p.Thr214=
XM_017011290.2:c.642A>G XP_016866779.1:p.Thr214=
XM_017011291.2:c.642A>G XP_016866780.1:p.Thr214=
XM_017011292.2:c.642A>G XP_016866781.1:p.Thr214=
XM_017011293.2:c.588A>G XP_016866782.1:p.Thr196=
XM_017011294.2:c.642A>G XP_016866783.1:p.Thr214=
XM_017011295.2:c.642A>G XP_016866784.1:p.Thr214=
XM_017011296.2:c.642A>G XP_016866785.1:p.Thr214=
XM_017011297.2:c.588A>G XP_016866786.1:p.Thr196=
XM_017011298.2:c.642A>G XP_016866787.1:p.Thr214=
XM_024446545.1:c.642A>G XP_024302313.1:p.Thr214=
XM_024446546.1:c.642A>G XP_024302314.1:p.Thr214=
XM_024446547.1:c.642A>G XP_024302315.1:p.Thr214=
ENST00000211379.9:c.642A>G ENSP00000211379.5:p.Thr214=
ENST00000362049.10:c.642A>G ENSP00000354875.6:p.Thr214=
ENST00000375964.10:c.660A>G ENSP00000365131.5:p.Thr220=
ENST00000375976.8:c.642A>G ENSP00000365143.4:p.Thr214=
ENST00000424176.5:c.588A>G ENSP00000391783.1:p.Thr196=
ENST00000424480.5:c.642A>G ENSP00000411043.1:p.Thr214=
ENST00000428326.5:c.642A>G ENSP00000413561.1:p.Thr214=
ENST00000433828.5:c.642A>G ENSP00000388244.1:p.Thr214=
ENST00000434444.5:c.588A>G ENSP00000394856.1:p.Thr196=
ENST00000435080.5:c.642A>G ENSP00000411083.1:p.Thr214=
ENST00000437771.5:c.642A>G ENSP00000397978.1:p.Thr214=
ENST00000439687.6:c.642A>G ENSP00000402856.2:p.Thr214=
ENST00000441054.5:c.588A>G ENSP00000406302.1:p.Thr196=
ENST00000451898.5:c.588A>G ENSP00000391613.1:p.Thr196=
ENST00000452994.5:c.642A>G ENSP00000404971.1:p.Thr214=
ENST00000456622.5:c.588A>G ENSP00000401031.1:p.Thr196=