Canonical Allele Identifier: CA406607631
Community Standard Title: NM_001394372.1(BICRA):c.3529C>T (p.Arg1177Ter)
Gene: BICRA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47699339C>T , CM000681.2:g.47699339C>T GRCh38
NC_000019.9:g.48202596C>T , CM000681.1:g.48202596C>T GRCh37
NC_000019.8:g.52894408C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001394372.1:c.3529C>T MANE Select NP_001381301.1:p.Arg1177Ter
ENST00000594866.3:c.3529C>T MANE Select ENSP00000469738.2:p.Arg1177Ter
NM_015711.3:c.3529C>T NP_056526.3:p.Arg1177Ter
ENST00000396720.7:c.3529C>T ENSP00000379946.2:p.Arg1177Ter
ENST00000614245.1:c.3373C>T ENSP00000480219.1:p.Arg1125Ter
ENST00000614245.2:c.2803C>T ENSP00000480219.2:p.Arg935Ter
XM_005258833.3:c.3529C>T XP_005258890.1:p.Arg1177Ter
XM_005258833.4:c.3529C>T XP_005258890.1:p.Arg1177Ter
XM_006723180.2:c.2449C>T XP_006723243.1:p.Arg817Ter
XM_006723180.3:c.2449C>T XP_006723243.1:p.Arg817Ter
XM_011526882.1:c.3391C>T XP_011525184.1:p.Arg1131Ter
XM_011526882.2:c.3391C>T XP_011525184.1:p.Arg1131Ter
XM_011526883.1:c.3352C>T XP_011525185.1:p.Arg1118Ter
XM_011526883.2:c.3352C>T XP_011525185.1:p.Arg1118Ter