Canonical Allele Identifier: CA1932270768

Gene: BTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.101554012C= , CM000672.2:g.101554012C=	GRCh38
NC_000010.10:g.103313769C= , CM000672.1:g.103313769C=	GRCh37
NC_000010.9:g.103303759C=	NCBI36
NG_009234.1:g.204945C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370187.8:c.*889C= MANE Select	ENSP00000359206.3:n.*889C=
ENST00000370187.7:c.*889C=	ENSP00000359206.3:n.*889C=
ENST00000393441.8:c.*889C=	ENSP00000377088.5:n.*889C=
ENST00000408038.6:c.*889C=	ENSP00000385339.2:n.*889C=
NM_001256856.1:c.*889C=	NP_001243785.1:n.*889C=
NM_003939.4:c.*889C=	NP_003930.1:n.*889C=
NM_033637.3:c.*889C=	NP_378663.1:n.*889C=
XM_005270264.2:c.*889C=	XP_005270321.1:n.*889C=
XM_006718054.2:c.*889C=	XP_006718117.1:n.*889C=
XM_011540320.1:c.*889C=	XP_011538622.1:n.*889C=
XM_011540320.2:c.*889C=	XP_011538622.1:n.*889C=
XM_017016870.1:c.*889C=	XP_016872359.1:n.*889C=
XM_017016871.1:c.*889C=	XP_016872360.1:n.*889C=
XM_017016872.1:c.*889C=	XP_016872361.1:n.*889C=
XM_017016873.2:c.*889C=	XP_016872362.1:n.*889C=
XM_017016874.1:c.*889C=	XP_016872363.1:n.*889C=
XM_024448246.1:c.*889C=	XP_024304014.1:n.*889C=
XM_024448247.1:c.*889C=	XP_024304015.1:n.*889C=
XR_001747256.1:n.3058C=
NM_033637.4:c.*889C= MANE Select	NP_378663.1:n.*889C=
NM_003939.5:c.*889C=	NP_003930.1:n.*889C=
NM_001256856.2:c.*889C=	NP_001243785.1:n.*889C=