Canonical Allele Identifier: CA2339526614
Gene: BICRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47680423C= , CM000681.2:g.47680423C= GRCh38
NC_000019.9:g.48183680C= , CM000681.1:g.48183680C= GRCh37
NC_000019.8:g.52875492C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000594866.3:c.1253C= MANE Select ENSP00000469738.2:p.Ala418=
ENST00000614245.2:c.527C= ENSP00000480219.2:p.Ala176=
ENST00000396720.7:c.1253C= ENSP00000379946.2:p.Ala418=
ENST00000614245.1:c.1097C= ENSP00000480219.1:p.Ala366=
NM_015711.3:c.1253C= NP_056526.3:p.Ala418=
XM_005258833.3:c.1253C= XP_005258890.1:p.Ala418=
XM_006723180.2:c.1253C= XP_006723243.1:p.Ala418=
XM_011526882.1:c.1115C= XP_011525184.1:p.Ala372=
XM_011526883.1:c.1253C= XP_011525185.1:p.Ala418=
XM_005258833.4:c.1253C= XP_005258890.1:p.Ala418=
XM_006723180.3:c.1253C= XP_006723243.1:p.Ala418=
XM_011526882.2:c.1115C= XP_011525184.1:p.Ala372=
XM_011526883.2:c.1253C= XP_011525185.1:p.Ala418=
NM_001394372.1:c.1253C= MANE Select NP_001381301.1:p.Ala418=