Canonical Allele Identifier: CA2586097337

Gene: BICRA

Linked Data

• gnomAD v4: 19-47680411-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47680415del , CM000681.2:g.47680415del	GRCh38
NC_000019.9:g.48183672del , CM000681.1:g.48183672del	GRCh37
NC_000019.8:g.52875484del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000594866.3:c.1245del MANE Select	ENSP00000469738.2:p.Ala416ArgfsTer28
ENST00000614245.2:c.519del	ENSP00000480219.2:p.Ala174ArgfsTer28
ENST00000396720.7:c.1245del	ENSP00000379946.2:p.Ala416ArgfsTer28
ENST00000614245.1:c.1089del	ENSP00000480219.1:p.Ala364ArgfsTer28
NM_015711.3:c.1245del	NP_056526.3:p.Ala416ArgfsTer28
XM_005258833.3:c.1245del	XP_005258890.1:p.Ala416ArgfsTer28
XM_006723180.2:c.1245del	XP_006723243.1:p.Ala416ArgfsTer28
XM_011526882.1:c.1107del	XP_011525184.1:p.Ala370ArgfsTer28
XM_011526883.1:c.1245del	XP_011525185.1:p.Ala416ArgfsTer28
XM_005258833.4:c.1245del	XP_005258890.1:p.Ala416ArgfsTer28
XM_006723180.3:c.1245del	XP_006723243.1:p.Ala416ArgfsTer28
XM_011526882.2:c.1107del	XP_011525184.1:p.Ala370ArgfsTer28
XM_011526883.2:c.1245del	XP_011525185.1:p.Ala416ArgfsTer28
NM_001394372.1:c.1245del MANE Select	NP_001381301.1:p.Ala416ArgfsTer28