Canonical Allele Identifier: CA2339526565
Gene: BICRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47680339A= , CM000681.2:g.47680339A= GRCh38
NC_000019.9:g.48183596A= , CM000681.1:g.48183596A= GRCh37
NC_000019.8:g.52875408A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000594866.3:c.1169A= MANE Select ENSP00000469738.2:p.Gln390=
ENST00000614245.2:c.443A= ENSP00000480219.2:p.Gln148=
ENST00000396720.7:c.1169A= ENSP00000379946.2:p.Gln390=
ENST00000614245.1:c.1013A= ENSP00000480219.1:p.Gln338=
NM_015711.3:c.1169A= NP_056526.3:p.Gln390=
XM_005258833.3:c.1169A= XP_005258890.1:p.Gln390=
XM_006723180.2:c.1169A= XP_006723243.1:p.Gln390=
XM_011526882.1:c.1031A= XP_011525184.1:p.Gln344=
XM_011526883.1:c.1169A= XP_011525185.1:p.Gln390=
XM_005258833.4:c.1169A= XP_005258890.1:p.Gln390=
XM_006723180.3:c.1169A= XP_006723243.1:p.Gln390=
XM_011526882.2:c.1031A= XP_011525184.1:p.Gln344=
XM_011526883.2:c.1169A= XP_011525185.1:p.Gln390=
NM_001394372.1:c.1169A= MANE Select NP_001381301.1:p.Gln390=