Canonical Allele Identifier: CA2397726927
Gene: BCR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23308849_23308853delinsAAGTT , CM000684.2:g.23308849_23308853delinsAAGTT GRCh38
NC_000022.10:g.23651036_23651040delinsAAGTT , CM000684.1:g.23651036_23651040delinsAAGTT GRCh37
NC_000022.9:g.21981036_21981040delinsAAGTT NCBI36
NG_009244.1:g.133485_133489delinsAAGTT
NG_009244.2:g.133485_133489delinsAAGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000305877.13:c.3013-575_3013-571delinsAAGTT MANE Select ENSP00000303507.8:n.3013-575_3013-571delinsAAGTT
ENST00000305877.12:c.3013-575_3013-571delinsAAGTT ENSP00000303507.8:n.3013-575_3013-571delinsAAGTT
ENST00000359540.7:c.2881-575_2881-571delinsAAGTT ENSP00000352535.3:n.2881-575_2881-571delinsAAGTT
ENST00000398512.9:c.1709-575_1709-571delinsAAGTT ENSP00000381524.6:n.1709-575_1709-571delinsAAGTT
ENST00000419722.6:n.238-575_238-571delinsAAGTT
ENST00000475025.5:n.87-575_87-571delinsAAGTT
ENST00000478978.5:n.294-575_294-571delinsAAGTT
NM_004327.3:c.3013-575_3013-571delinsAAGTT NP_004318.3:n.3013-575_3013-571delinsAAGTT
NM_021574.2:c.2881-575_2881-571delinsAAGTT NP_067585.2:n.2881-575_2881-571delinsAAGTT
NM_004327.4:c.3013-575_3013-571delinsAAGTT MANE Select NP_004318.3:n.3013-575_3013-571delinsAAGTT
NM_021574.3:c.2881-575_2881-571delinsAAGTT NP_067585.2:n.2881-575_2881-571delinsAAGTT