Canonical Allele Identifier: CA658933502

Gene: BTRC

Linked Data

• dbSNP Id: rs1397335047
• MyVariant Identifiers: chr10:g.103313646C>A (hg19) ; chr10:g.101553889C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101553889C>A , CM000672.2:g.101553889C>A	GRCh38
NC_000010.10:g.103313646C>A , CM000672.1:g.103313646C>A	GRCh37
NC_000010.9:g.103303636C>A	NCBI36
NG_009234.1:g.204822C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370187.8:c.*766C>A MANE Select	ENSP00000359206.3:n.*766C>A
ENST00000370187.7:c.*766C>A	ENSP00000359206.3:n.*766C>A
ENST00000393441.8:c.*766C>A	ENSP00000377088.5:n.*766C>A
ENST00000408038.6:c.*766C>A	ENSP00000385339.2:n.*766C>A
NM_001256856.1:c.*766C>A	NP_001243785.1:n.*766C>A
NM_003939.4:c.*766C>A	NP_003930.1:n.*766C>A
NM_033637.3:c.*766C>A	NP_378663.1:n.*766C>A
XM_005270264.2:c.*766C>A	XP_005270321.1:n.*766C>A
XM_006718054.2:c.*766C>A	XP_006718117.1:n.*766C>A
XM_011540320.1:c.*766C>A	XP_011538622.1:n.*766C>A
XM_011540320.2:c.*766C>A	XP_011538622.1:n.*766C>A
XM_017016870.1:c.*766C>A	XP_016872359.1:n.*766C>A
XM_017016871.1:c.*766C>A	XP_016872360.1:n.*766C>A
XM_017016872.1:c.*766C>A	XP_016872361.1:n.*766C>A
XM_017016873.2:c.*766C>A	XP_016872362.1:n.*766C>A
XM_017016874.1:c.*766C>A	XP_016872363.1:n.*766C>A
XM_024448246.1:c.*766C>A	XP_024304014.1:n.*766C>A
XM_024448247.1:c.*766C>A	XP_024304015.1:n.*766C>A
XR_001747256.1:n.2935C>A
NM_033637.4:c.*766C>A MANE Select	NP_378663.1:n.*766C>A
NM_003939.5:c.*766C>A	NP_003930.1:n.*766C>A
NM_001256856.2:c.*766C>A	NP_001243785.1:n.*766C>A