Canonical Allele Identifier: CA13656499

Gene: BCL7A

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.122046634G>A , CM000674.2:g.122046634G>A	GRCh38
NC_000012.11:g.122484540G>A , CM000674.1:g.122484540G>A	GRCh37
NC_000012.10:g.120968923G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261822.5:c.439+2581G>A MANE Select	ENSP00000261822.5:n.439+2581G>A
ENST00000261822.4:c.439+2581G>A	ENSP00000261822.4:n.439+2581G>A
ENST00000538010.5:c.439+2581G>A	ENSP00000445868.1:n.439+2581G>A
NM_001024808.2:c.439+2581G>A	NP_001019979.1:n.439+2581G>A
NM_020993.4:c.439+2581G>A	NP_066273.1:n.439+2581G>A
NM_001024808.3:c.439+2581G>A MANE Select	NP_001019979.1:n.439+2581G>A
NM_020993.5:c.439+2581G>A	NP_066273.1:n.439+2581G>A