Canonical Allele Identifier: CA658933587

Gene: BTRC

Linked Data

• dbSNP Id: rs1292137354
• gnomAD v3: 10-101554014-CTCTT-C
• gnomAD v4: 10-101554014-CTCTT-C
• MyVariant Identifiers: chr10:g.103313772_103313775del (hg19) ; chr10:g.101554015_101554018del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101554019_101554022del , CM000672.2:g.101554019_101554022del	GRCh38
NC_000010.10:g.103313776_103313779del , CM000672.1:g.103313776_103313779del	GRCh37
NC_000010.9:g.103303766_103303769del	NCBI36
NG_009234.1:g.204952_204955del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370187.8:c.*896_*899del MANE Select	ENSP00000359206.3:n.*896_*899del
ENST00000370187.7:c.*896_*899del	ENSP00000359206.3:n.*896_*899del
ENST00000393441.8:c.*896_*899del	ENSP00000377088.5:n.*896_*899del
ENST00000408038.6:c.*896_*899del	ENSP00000385339.2:n.*896_*899del
NM_001256856.1:c.*896_*899del	NP_001243785.1:n.*896_*899del
NM_003939.4:c.*896_*899del	NP_003930.1:n.*896_*899del
NM_033637.3:c.*896_*899del	NP_378663.1:n.*896_*899del
XM_005270264.2:c.*896_*899del	XP_005270321.1:n.*896_*899del
XM_006718054.2:c.*896_*899del	XP_006718117.1:n.*896_*899del
XM_011540320.1:c.*896_*899del	XP_011538622.1:n.*896_*899del
XM_011540320.2:c.*896_*899del	XP_011538622.1:n.*896_*899del
XM_017016870.1:c.*896_*899del	XP_016872359.1:n.*896_*899del
XM_017016871.1:c.*896_*899del	XP_016872360.1:n.*896_*899del
XM_017016872.1:c.*896_*899del	XP_016872361.1:n.*896_*899del
XM_017016873.2:c.*896_*899del	XP_016872362.1:n.*896_*899del
XM_017016874.1:c.*896_*899del	XP_016872363.1:n.*896_*899del
XM_024448246.1:c.*896_*899del	XP_024304014.1:n.*896_*899del
XM_024448247.1:c.*896_*899del	XP_024304015.1:n.*896_*899del
XR_001747256.1:n.3065_3068del
NM_033637.4:c.*896_*899del MANE Select	NP_378663.1:n.*896_*899del
NM_003939.5:c.*896_*899del	NP_003930.1:n.*896_*899del
NM_001256856.2:c.*896_*899del	NP_001243785.1:n.*896_*899del