Canonical Allele Identifier: CA2339526664
Gene: BICRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47680521C= , CM000681.2:g.47680521C= GRCh38
NC_000019.9:g.48183778C= , CM000681.1:g.48183778C= GRCh37
NC_000019.8:g.52875590C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000594866.3:c.1351C= MANE Select ENSP00000469738.2:p.Leu451=
ENST00000614245.2:c.625C= ENSP00000480219.2:p.Leu209=
ENST00000396720.7:c.1351C= ENSP00000379946.2:p.Leu451=
ENST00000614245.1:c.1195C= ENSP00000480219.1:p.Leu399=
NM_015711.3:c.1351C= NP_056526.3:p.Leu451=
XM_005258833.3:c.1351C= XP_005258890.1:p.Leu451=
XM_006723180.2:c.1351C= XP_006723243.1:p.Leu451=
XM_011526882.1:c.1213C= XP_011525184.1:p.Leu405=
XM_011526883.1:c.1351C= XP_011525185.1:p.Leu451=
XM_005258833.4:c.1351C= XP_005258890.1:p.Leu451=
XM_006723180.3:c.1351C= XP_006723243.1:p.Leu451=
XM_011526882.2:c.1213C= XP_011525184.1:p.Leu405=
XM_011526883.2:c.1351C= XP_011525185.1:p.Leu451=
NM_001394372.1:c.1351C= MANE Select NP_001381301.1:p.Leu451=