Canonical Allele Identifier: CA2339526564

Gene: BICRA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47680336A= , CM000681.2:g.47680336A=	GRCh38
NC_000019.9:g.48183593A= , CM000681.1:g.48183593A=	GRCh37
NC_000019.8:g.52875405A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000594866.3:c.1166A= MANE Select	ENSP00000469738.2:p.Gln389=
ENST00000614245.2:c.440A=	ENSP00000480219.2:p.Gln147=
ENST00000396720.7:c.1166A=	ENSP00000379946.2:p.Gln389=
ENST00000614245.1:c.1010A=	ENSP00000480219.1:p.Gln337=
NM_015711.3:c.1166A=	NP_056526.3:p.Gln389=
XM_005258833.3:c.1166A=	XP_005258890.1:p.Gln389=
XM_006723180.2:c.1166A=	XP_006723243.1:p.Gln389=
XM_011526882.1:c.1028A=	XP_011525184.1:p.Gln343=
XM_011526883.1:c.1166A=	XP_011525185.1:p.Gln389=
XM_005258833.4:c.1166A=	XP_005258890.1:p.Gln389=
XM_006723180.3:c.1166A=	XP_006723243.1:p.Gln389=
XM_011526882.2:c.1028A=	XP_011525184.1:p.Gln343=
XM_011526883.2:c.1166A=	XP_011525185.1:p.Gln389=
NM_001394372.1:c.1166A= MANE Select	NP_001381301.1:p.Gln389=